- Open Access
Quality of life of children with achondroplasia and their parents - a German cross-sectional study
Orphanet Journal of Rare Diseasesvolume 14, Article number: 194 (2019)
Achondroplasia is the most common form of disproportionate short stature and might affect not only the quality of life of the affected child but also that of the parents.
We aimed to investigate the quality of life of children with achondroplasia from child- and parent perspective as well as the parental quality of life.
Forty-seven children with achondroplasia and 73 parents from a German patient organization participated. We assessed children’s quality of life using the generic Peds QL 4.0™ as self-reports for children aged 8–14 and parent-reports for children aged 4–14 years. Parental quality of life we assessed using the short-form 8-questionnaire.
Children with achondroplasia showed significantly lower quality of life scores compared to a healthy reference population from both the child- and parent-report (p = ≤.01), except the child-report of the emotional domain (t (46) = − 1.73, p = .09). Parents reported significantly lower mental health in comparison with a German reference population (t (72) = 5.64, p ≤ .01) but no lower physical health (t (72) = .20, p = .85). While the parental quality of life was a significant predictor of parent-reported children’s quality of life (F (6,66) = 2.80, p = .02), it was not for child-reported children’s quality of life (F (6,66) = .92, p = .49).
Achondroplasia is chronically debilitating. Thus special efforts are needed to address patients’ and parent’s quality of life needs. This special health condition may influence the daily life of the entire family because they have to adapt to the child’s particular needs. Therefore, clinicians should not only focus on the child’s quality of life but also those of the parents.
Achondroplasia is the most recognizable form of short stature , characterized by disproportionate short stature with prevalence rates about 1:10,000 to 1:30,000 per live births [2, 3]. The cause of achondroplasia was identified to be a gain-of-function mutations in the gene for the fibroblast growth factor receptor 3 (FGFR-3) and is known to be an autosomal dominant trait [1, 4]. Achondroplasia is characterized by short stature, short limbs, and rhizomelic disproportion, macrocephaly, and midfacial retrusion. Other characteristics are a small chest, thoracolumbar kyphosis, lumbar hyperlordosis, limited elbow extension, short fingers, and trident configuration of the hands. Patients may also show hypermobile hips and knees, bowing of the mesial segment of the legs as well as hypotonia . Affected patients experience various orthopedic and neurological complications and might face multiple medical and non-medical challenges in their daily life [5,6,7,8].
Adult patients reported physical and mental impairments as well as lower quality of life and lower self-esteem than healthy relatives [9, 10]. By the same time, relatives rated the perception of the condition more frequently as serious or lethal than the affected adults . Furthermore, stigmatization, isolation, and difficulties in accessing adequate healthcare increase the risk for problems in psychosocial health [11, 12].
Therefore, quality of life as a central patient-reported outcome measure became an important health indicator in the context of the care of chronically ill patients [13, 14]. According to this relevance, we have developed and tested a patient-reported outcome instrument for young people with achondroplasia, emphasizing the benefits of this disease-specific instrument [15, 16].
Previous studies reported a significantly reduced quality of life of children with chronic health conditions from both the child and parent perspective in comparison with healthy reference populations [17, 18]. At the same time, other studies reported no differences in quality of life of chronically ill children, compared to healthy peers [19, 20]. In contrast to children with endocrine short-stature, children with achondroplasia reported significantly lower quality of life [8, 12, 19]. In particular, young patients with achondroplasia showed the lowest quality of life scores in the physical domain, the highest quality of life scores in the emotional domain [6, 8, 10, 12, 21].
Results from other studies reveal that young patients rate their quality of life significantly higher than their parents, although the age of the patients can affect the perceived quality of life [8, 12, 21]. The fact that a positive attitude towards body height and weight is significantly associated with a better psychological status has been reported in studies with clinical populations [8, 12, 19]. Besides, results reveal interventions can have a positive effect on the quality of life of young patients with achondroplasia [12, 19].
The impact of chronic illness on both the children themselves and their families has been recognized as an essential research area [22,23,24]. While the child’s health condition can affect the parental quality of life negatively, competent parenting is regarded to have the potential to positively affect children’s adjustment to their chronic illness .
Currently, research on the quality of life of parents of chronically ill children shows no consistent results. While the majority of studies reported limitations in quality of life of parents of chronically ill children [26,27,28,29], other studies have shown no significant association between a chronic health condition of a child and parental quality of life [30,31,32,33]. We have already studied the quality of life of children, adolescents and young adults with achondroplasia in previous studies [8, 19, 21, 34] in order to  understand the patients’ perception of their quality of life,  identify psychosocial and clinical predictors for intervention planning and  evaluate the effect of a novel intervention [8, 12, 19, 21]. The qualitative analyses showed, that parents – especially when receiving the diagnosis – feel helpless and overwhelmed independently from prenatal and postnatal diagnoses . Gollust, Thompson  showed that adults with higher quality of life were more likely to decline prenatal screening than those with lower quality of life. However, we did not yet consider the quality of life of parents with children with achondroplasia.
In the current study, we aimed  to investigate the effects of achondroplasia on the quality of life of children with achondroplasia from child and parent perspective,  to investigate the quality of life of the parents and  to explore associations between parental quality of life and children’s quality of life. We hypothesize that the quality of life of children born with achondroplasia and the parental quality of life will be significantly reduced compared to a reference population. We assume height will be an important variable to explain both, the self and parent-reported children’s quality of life, while parental quality of life will primarily contribute to explain parent reported children’s quality of life.
The present study is part of the Achondroplasia Personal Life Scale Experience Scale study that focused on developing a questionnaire to assess quality of life and functioning in children and adolescents with achondroplasia based on the International Classification of Functioning, Disability, and Health . The current analyses used data from the field test phase. We enrolled families (one parent per child) through the German Association for People of Short Stature and their Families if they met the inclusion and exclusion criteria (Fig. 1). The German Association for People of Short Stature and their Families is a national patient organization focusing on all kinds of short stature and offering many support options such as contact to specialized physicians, orthopedists, psychologists as well as frequent membership meetings to come together with other families with short-statured children. The patient organization contacted only families with a clinical diagnosis of achondroplasia and no other known serious illnesses. Families received detailed information about the aims of this study in a written form. We obtained ethic approval to conduct the study from the Ethical Review Board of Magdeburg, Germany (45/15) before we started.
We have sent out questionnaires for children aged 8 to 14 years and parents of children aged 5 to 14 years in October 2015 by mail to all families that had given their written consent. Data collection took place over six months in which a maximum of two reminders was sent out.
We measured children’s QoL using the generic PedsQL 4.0™ questionnaire. This instrument is available in self-report for children aged eight years and over and in parent-report for younger children. The PedsQL 4.0™ is composed of 23 items rated on a 5-point Likert scale and comprises four domains (Physical Functioning, Emotional Functioning, Social Functioning, and School Functioning) as well as three overall scores (Psychosocial Health Summary Score, Physical Health Summary Score, and Total Score). Good reliability was found in the current sample, with Cronbach’s Alpha values ranging from α = .75 (school; parent-report) to α = .94 (total score; self-report). References from a healthy pediatric sample are available for self- and parent-reports [17, 36].
We measured parental quality of life using the Short-Form-8 questionnaire (SF-8), which is a short form of the SF-36, an internationally used generic quality of life instrument. In the current sample, the total scores of the SF-8 showed good reliability for the physical component score with Cronbach’s α = .86 and the mental component score with Cronbach’s α = .85. Gender- and age-adjusted German norm-based data are available .
Finally, we collected sociodemographic and clinical data from the parents. The standard deviation score (SDS) of height was calculated using German reference values .
We performed bivariate analyses using Students t-Test. To determine the degree of convergence between parental quality of life and children’s quality of life, we calculated paired Pearson correlations. We performed multiple linear regression analyses with children’s quality of life (self-report and parent-report) as an endpoint.
For all statistical analyses, we used the IBM Statistical Package for Social Sciences Statistics version 21.0. Except for sociodemographic and clinical variables, we replaced missing values by the individual mean score for each variable, if missing data were random and less than 20% of the values. The significance level was set to be less than .05 (p ≤ .05).
A total of 73 families participated, including 73 parent-reports (children aged 5–14 years) and 47 child-reports (children aged 8–14 years) (Table 1).
Children’s quality of life
In the sample, parents of children with achondroplasia reported significantly lower quality of life scores for their children compared to a healthy reference population for all domains (p ≤ .01) . The children themselves also rated their quality of life significantly lower compared to a healthy reference population for all domains (p ≤ .02) with the exception of the domain emotional (t (46) = − 1.73, p = .09) (Table 2).
Parental quality of life
We compared the quality of life scores of the parents of this study sample with norm values of a German reference population and found significantly lower scores for the mental component score (t (72) = 5.64, p ≤ .01), but we detected no differences for the physical component score (t (72) = .20, p = .85) Table 2).
Correlations between children’s quality of life and parental quality of life
We show paired Pearson correlations between parental quality of life (physical component score and mental component score), children’s self-reported quality of life and children’s parent-reported quality of life in (Figs. 2 and 3). The values indicate positive correlations with the relatively highest convergence between children’s parent-reported generic quality of life and parental physical quality of life and (r = .38; p ≤ .01) as well as children’s parent-reported quality of life and parental mental quality of life (r = .32; p ≤ .01). Correlation between child-reported children’s quality of life and parental physical quality of life also reached the significance level (r = .33; p = .02). Child-reported children’s quality of life and parental mental quality of life did not show any significant correlation (r = .24; p = .11).
With the regression analyses, we demonstrated that our model predicts significantly on the parent-reported children’s quality of life (F (6,66) = 2.80, p = .02). Parental physical quality of life (β = .25, p = .04) and parental mental quality of life (β = .30, p = .02) showed to be significant predictors of parent-reported children’s quality of life. The same model did not contribute to explaining a substantial variance of child-reported children’s quality of life (F (6,66) = .92, p = .49). For sociodemographic and clinical variables, we did not find any effect on children’s quality of life, neither for the child-reported nor for the parent-reported children’s quality of life (Table 3).
To our knowledge, this is the first study focusing on the quality of life of children diagnosed with achondroplasia, the quality of life of parents of children with achondroplasia as well as correlations and determinants of children’s quality of life from both perspectives – child-reported quality of life and parent-reported quality of life. Both the children with achondroplasia and their parents rated the children’s quality of life significantly lower compared to a healthy reference population. We did not find any significant differences in the emotional domain in the child-report. The emotional domain includes expressions like feelings of anxiety, sadness, anger, worry, and sleep difficulties. In this domain, the children with achondroplasia reported quality of life comparable to a healthy reference population. A German-Swedish study is investigating the quality of life of children born with esophageal atresia using the PedsQL 4.0™ even reported a significantly higher quality of life score on the emotional scale compared to a healthy reference population . Patients with chronic illness showed improved coping with everyday stressors compared to the healthy controls . Similarly, Rohenkohl, Bullinger  showed that children with achondroplasia reported the highest quality of life scores in the emotional domain. The affected children may have learned to accept themselves as they are and to be satisfied with themselves - even if they experience significant limitations in the domain of physical quality of life, as well as in the domains of school and social life. While these capacities and environments cannot be influenced by the children, the intrapersonal emotional attitude towards oneself can be modulated and strengthened by suitable coping strategies and social support from parents and friends.
Results of our previous study, shows that participants of interventions, which are based on the specific needs of the target population, resulted in a significant increase in quality of life in comparison to non-participating patients [12, 34]. Our current sample consists of members of an active patient organization, which offers frequent regional and national membership meetings as well as intensive support through employees and volunteers. This support system might have an impact on our results – especially on the copings strategies used by affected children as well as their parents and their social and emotional quality of life.
The reduced quality of life of children with achondroplasia can be explained by the physical restrictions and limitations as well as various challenges in daily life reported by children, adolescents and young adults with achondroplasia in focus group discussions and was confirmed by their parents’ perception . Despite the physical demands that result from this for the parents, the parents of our sample showed no restrictions compared to a representative comparison group about their physical quality of life. Similarly, parents of children born with esophageal atresia reported no physical quality of life restriction compared with a reference population . In particular, limitations of motor skills as well as practical life skills contributed significantly to an increased parental burden [41, 42]. In addition to the above mentioned physical strains, parents of children with chronic health conditions are also exposed to other stressors, such as stigmatization, feelings of guilt, and fears of the future, which can have a negative impact on the mental health of the parents . The present sample of parents of children with achondroplasia highlighted this burden with a significantly reduced mental quality of life compared to a German reference group. These findings confirm the results of a meta-analysis from Teubert and Pinquart , in which they described the burden and impairments of parents of chronically ill children compared to parents of healthy children. Also, parents of children with rare health conditions reported this significantly reduced mental quality of life . While the parents of the children and adolescents with achondroplasia in this sample reported reduced mental quality of life, parents of short statured children and adolescents diagnosed with endocrine short stature showed no restrictions of their quality of life compared to a healthy reference population. However, in the study, no differentiation was made between physical and mental quality of life . We assume that the form of short stature (e.g. growth hormone deficiency and small for gestational age versus achondroplasia) plays an important role not on the children’s quality of life  but also on the perception of parental quality of life. Children with endocrine short stature are much less likely to be stigmatized than children with achondroplasia. Furthermore children with achondroplasia often suffer from many complications and concomitant limitations in everyday life. Accordingly parents have to afford more care for children with achondroplasia than for children with endocrine short stature.
The correlations between parent-reported children’s quality of life and parental quality of life showed significant results for both parental physical quality of life and parental mental quality of life. The higher the parental quality of life, the higher the parent-reported children’s quality of life. This also shows the correlation between parental physical quality of life and child-reported children’s quality of life. However, we found no significant association for parental mental quality of life and child-reported quality of life.  showed similar findings and reported significant correlations between parental quality of life and parent-reported children’s quality of life for families with children born with esophageal atresia.
Sociodemographic and clinical characteristics of the children showed no effect on the children’s quality of life for neither the child-report nor the parent-report. However, parental physical and mental quality of life predicted the parent-reported children’s quality of life significantly. This stresses the importance of the parental perception of their children’s quality of life, depending on the parental physical and mental constitution.
The influence of the parental quality of life on the parental assessment of the children’s quality of life should be investigated in future research to identify relevant factors that affect the parental ability to assess their child’s quality of life. The different roles in caregiving and stressors of mothers and fathers should be considered when investigating the caregiving burden of parents whose children are diagnosed with a rare disorder such as achondroplasia. An increased understanding of the specific situation of parents of a chronically ill child will help to obtain insight starting points for interventions, to provide tailored support for these parents. As parents are able to improve their adjustment to the illness of their child and to increase their own quality of life, their children’s well-being and health-related outcomes may improve .
For clinicians, it is therefore important to assess children’s quality of life from all possible perspectives - from the child as well as both parents – together with the parental quality of life to obtain a comprehensive view of the situation and to include all reports in decision-making processes.
Limitations to this study include the recruitment of a highly selective sample (drawn only from a national patient organization), the lack of data about non-participants, and the lack of data pertaining to the sociodemographic background of the families. Clinical data were also reported by parents only. In addition to these weaknesses, more mothers participated in this study than fathers. We enrolled only one parent per child in this study. For future research, it would be useful to include both parents to comprehensively represent the family situation and to be able to reveal possible differences in parental perception. Rare disorders, such as achondroplasia, are chronically debilitating. Thus special efforts are needed to address patients’ and parent’s needs. The results of this paper confirm a reduced quality of life in affected children. We would recommend that such quality of life assessment should not only include self- and parent-reported data as complementary sources of information; they should also consider the family context .
Our results reveal that the parents of this study sample showed a reduced mental quality of life - regardless of the height of their child. Thus, it is important to recognize that pediatric short stature affects not only the child but the family as a whole .
The diagnosis of achondroplasia and its consequences may influence the daily life of the entire family because they have to adapt to the child’s special needs. A straightforward implication of our study is the need to assess the child’s as well as the parental quality of life to develop family-centered psychosocial interventions, thus improving both children’s and parents’ adaptation outcomes.
Achondroplasia is chronically debilitating. Thus special efforts are needed to address patients’ and parent’s quality of life needs. The chronic health condition may influence the daily life of the entire family because they have to adapt to the child’s special needs. Although young patients report higher quality of life in the self-report their parents, the comparisons with healthy reference groups show reduced quality of life both from the perspective of the parents and the perspective of the affected children and adolescents. The reduced mental quality of life of parents refers to the burden for the parents that can result from the child’s chronic health condition. Since parental quality of life has a significant impact on the parent-reported quality of life of the children, clinicians should not only focus on the child’s quality of life but also those of the parents. Therefore, it is crucial to consider the psychosocial situation of the whole family.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Pauli RM. Achondroplasia: a comprehensive clinical review. Orphanet J Rare Dis. 2019;14:1):1.
Krakow D, Rimoin DL. The skeletal dysplasias. Genet Med. 2010;12(6):327–41.
Zabel B. FGFR3-Mutationen als Ursache von Skelletdysplasien der Achondroplasie-Gruppe - Aufklärung der gestörten Signalwege in der Wachstumsfuge [FGFR3-Mutations as a cause of skeletal dysplasia of the achondroplasia group - alucidation of disturbed signal pathways in the growth plate]. In: Mohnike K, Klingebiel KH, Vaupel N, Zabel B, editors. Achondroplasie und Hypochondroplasie - Diagnostik und Betreuung spezifischer Kleinwuchsformen [achondroplasia and Hypochondroplasia - diagnostic and care of specific forms of short stature]: ABW Wissensverlagsgesellschaft; 2013. p. 3–10.
Horton WA, Hall JG, Hecht JT. Achondroplasia. Lancet (London, England). 2007;370(9582):162–72.
Baujat G, Legeai-Mallet L, Finidori G, Cormier-Daire V, Le Merrer M. Achondroplasia. Best Pract Res Clin Rheumatol. 2008;22(1):3–18.
Dogba MJ, Rauch F, Douglas E, Bedos C. Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta. Health Qual Life Outcomes. 2014;12:151.
Hunter AG, Bankier A, Rogers JG, Sillence D, Scott CI Jr. Medical complications of achondroplasia: a multicentre patient review. J Med Genet. 1998;35(9):705–12.
Rohenkohl AC, Bullinger M, Quitmann J. Lebensqualität bei Kindern, Jugendlichen und jungen Erwachsenen mit Achondroplasie [quality of life in children, adolescents and young adults with achondroplasia]. Orthopade. 2015;44(3):212–8.
Gollust SE, Thompson RE, Gooding HC, Biesecker BB. Living with achondroplasia in an average-sized world: an assessment of quality of life. Am J Med Genet A. 2003;120a;(4):447–58.
Mahomed NN, Spellmann M, Goldberg MJ. Functional health status of adults with achondroplasia. Am J Med Genet. 1998;78(1):30–5.
Bogart KR, Irvin VL. Health-related quality of life among adults with diverse rare disorders. Orphanet J Rare Dis. 2017;12(1):177.
Witt S, Rohenkohl A, Bullinger M, Sommer R, Kahrs S, Klingebiel KH, et al. Understanding, assessing and improving health-related quality of life of young people with achondroplasia- a collaboration between a patient organization and academic medicine. Pediatr Endocrinol Rev. 2017;15(Suppl 1):109–18.
Ingerski LM, Modi AC, Hood KK, Pai AL, Zeller M, Piazza-Waggoner C, et al. Health-related quality of life across pediatric chronic conditions. J Pediatr. 2010;156(4):639–44.
Newacheck PW, Strickland B, Shonkoff JP, Perrin JM, McPherson M, McManus M, et al. An epidemiologic profile of children with special health care needs. Pediatrics. 1998;102(1 Pt 1):117–23.
Bloemeke J, Sommer R, Witt S, Dabs M, Badia FJ, Bullinger M, et al. Piloting and psychometric properties of a patient-reported outcome instrument for young people with achondroplasia based on the international classification of functioning disability and health: the achondroplasia personal life experience scale (APLES). Disabil Rehabil. 2019;41(15):1815–25.
Sommer R, Blomeke J, Dabs M, Witt S, Bullinger M, Quitmann J. An ICF-CY-based approach to assessing self- and observer-reported functioning in young persons with achondroplasia - development of the pilot version of the achondroplasia personal life experience scale (APLES). Disabil Rehabil. 2017;39(24):2499–503.
Varni JW, Limbers CA, Burwinkle TM. Impaired health-related quality of life in children and adolescents with chronic conditions: a comparative analysis of 10 disease clusters and 33 disease categories/severities utilizing the PedsQL 4.0 generic Core scales. Health Qual Life Outcomes. 2007;5:43.
Teubert D, Pinquart M. Belastungen der Eltern chronisch körperlich kranker kinder [burdens of parents of chronically physically ill children]. In: Pinquart M, editor. Wenn kinder und Jugendliche körperlich chronisch krank Sind: Psychische und soziale Entwicklung, Prävention, intervention [when children and adolescents are physically chronically ill: mental and social development, prevention, intervention]. Berlin, Heidelberg: Springer Berlin Heidelberg; 2013. p. 83–99.
Rohenkohl AS, R., Bestges S, Kahrs S, Klingebiel KH-B, M., Quitmann J. Leben mit Achondroplasie - Wie beurteilen junge menschen mit disproportioniertem Kleinwuchs ihre Lebensqualität und mit welchen Faktoren ist sie assoziiert? [living with achondroplasia - how do young persons with disproportional short stature rate their quality of life and which factors are associated with quality of life?]. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie 2015;43:433–41.
Silva N, Bullinger M, Quitmann J, Ravens-Sieberer U, Rohenkohl A. HRQoL of European children and adolescents with short stature as assessed with generic (KIDSCREEN) and chronic-generic (DISABKIDS) instruments. Expert Rev Pharmacoecon Outcomes Res. 2013;13(6):817–27.
Quitmann J, Witt S, Rohenkohl A, Bullinger M, Sommer R, Klingebiel R, et al. Lebensqualität junger menschen mit Achondroplasie. Qualitativer Vergleich der Perspektiven von Betroffenen und Eltern [quality of life of young patients with achondroplasia. Qualitative comparison of the perspectives of patients and parents]. Monatsschrift Kinderheilkunde. 2014;162(5):428–34.
Fitzgerald C, George S, Somerville R, Linnane B, Fitzpatrick P. Caregiver burden of parents of young children with cystic fibrosis. J Cyst Fibros. 2018;17(1):125–31.
Park E, Kim H, Steinhoff A. Health-related internet use by informal caregivers of children and adolescents: an integrative literature review. J Med Internet Res. 2016;18(3):e57.
Piran P, Khademi Z, Tayari N, Mansouri N. Caregiving burden of children with chronic diseases2017. 5380–7 p.
Logan DE, Scharff L. Relationships between family and parent characteristics and functional abilities in children with recurrent pain syndromes: an investigation of moderating effects on the pathway from pain to disability. J Pediatr Psychol. 2005;30(8):698–707.
Arafa MA, Zaher SR, El-Dowaty AA, Moneeb DE. Quality of life among parents of children with heart disease. Health Qual Life Outcomes. 2008;6:91.
Hatzmann J, Heymans HS, Ferrer-i-Carbonell A, van Praag BM, Grootenhuis MA. Hidden consequences of success in pediatrics: parental health-related quality of life--results from the care project. Pediatrics. 2008;122(5):e1030–8.
Lawoko S, Soares JJ. Quality of life among parents of children with congenital heart disease, parents of children with other diseases and parents of healthy children. Qual Life Res. 2003;12(6):655–66.
Witt S, Dellenmark-Blom M, Dingemann J, Dingemann C, Ure BM, Gomez B, et al. Quality of life in parents of children born with esophageal atresia. Eur J Pediatr Surg. 2018.
Berger ZE, Dalton LJ. Coping with a cleft: psychosocial adjustment of adolescents with a cleft lip and palate and their parents. Cleft Palate Craniofac J. 2009;46(4):435–43.
Hunfeld JA, Perquin CW, Duivenvoorden HJ, Hazebroek-Kampschreur AA, Passchier J, van Suijlekom-Smit LW, et al. Chronic pain and its impact on quality of life in adolescents and their families. J Pediatr Psychol. 2001;26(3):145–53.
Wiedebusch S, Konrad M, Foppe H, Reichwald-Klugger E, Schaefer F, Schreiber V, et al. Health-related quality of life, psychosocial strains, and coping in parents of children with chronic renal failure. Pediatr Nephrol (Berlin, Germany). 2010;25(8):1477–85.
Witt S, Bullinger M, Quitmann J. Emotionsregulation, psychische Auffälligkeiten und Lebensqualität von Kindern mit endokrinem Kleinwuchs [emotion regulation, strenghts and difficulties and quality of life of children with endocrine short stature]. Pädiatrische Praxis. 2018;90:200–10.
Rohenkohl A, Sommer R, Kahrs S, Bullinger M, Klingebiel K-H, Quitmann J. Evaluation eines selbsthilfegestützten psychosozialen Interventionsangebotes für kinder und Jugendliche mit disproportionalem Kleinwuchs [evaluation of a self-help supported counseling concept for children and adolescents with disproportional short stature]. Klin Padiatr. 2016;228(01):17–23.
Gollust SE, Thompson RE, Gooding HC, Biesecker BB. Living with achondroplasia: attitudes toward population screening and correlation with quality of life. Prenat Diagn. 2003;23(12):1003–8.
Varni JW, Limbers CA, Burwinkle TM. How young can children reliably and validly self-report their health-related quality of life?: an analysis of 8,591 children across age subgroups with the PedsQL 4.0 generic Core scales. Health Qual Life Outcomes. 2007;5:1.
Beierlein V, Morfled M, Bergelt C, Bullinger M, Brähler E. Messung der gesundheitsbezogenen Lebensqualität mit dem SF-8. Deutsche Normdaten aus einer repräsentativen schriftlichen Befragung [measuring health-related quality of life with the SF-8: German norms from a representative self-administered survey]. Diagnostica. 2012;58:145–53.
Kromeyer-Hauschild K, Wabitsch M, Kunze D, Geller F, Geiß HC, Hesse V, et al. Perzentile für den Body-mass-Index für das Kindes- und Jugendalter unter Heranziehung verschiedener deutscher Stichproben [Percentiles for the body mass index for children and adolescents, using German samples]. Monatsschrift Kinderheilkunde. 2001;149(8):807–18.
Flieder S, Dellenmark-Blom M, Witt S, Dingemann C, Quitmann JH, Jonsson L, et al. Generic health-related quality of life after repair of esophageal atresia and its determinants within a German-Swedish cohort. Eur J Pediatr Surg. 2019;29(1):75–84.
Hampel P, Rudolph H, Stachow R, Laß-Lentzsch A, Petermann F. Coping among children and adolescents with chronic illness. Anxiety Stress Coping. 2005;18(2):145–55.
Lindstrom C, Aman J, Norberg AL. Increased prevalence of burnout symptoms in parents of chronically ill children. Acta Paediatr (Oslo, Norway : 1992). 2010;99(3):427–32.
Tröster H, Bersch M, Ruppert S, Boenigk H-E. Determinanten der Belastung von Müttern mit anfallskranken Kindern [Determinants of stress in mothers of children with epilepsy]2000. 50–61 p.
Grootenhuis MA, Bronner MB. Paediatric illness! Family matters. Acta Paediatr (Oslo, Norway : 1992). 2009;98(6):940–1.
Quitmann J, Rohenkohl A, Sommer R, Bullinger M, Silva N. Explaining parent-child (dis) agreement in generic and short stature-specific health-related quality of life reports: do family and social relationships matter? Health Qual Life Outcomes. 2016;14(1):150.
Silva N, Bullinger M, Sommer R, Rohenkohl A, Witt S, Quitmann J. Children's psychosocial functioning and parents' quality of life in paediatric short stature: the mediating role of caregiving stress. Clin Psychol Psychother. 2018;25(1):e107–e18.
The authors would like to thank the staff from the German Association for People of Short Stature and their Families for their support and contributions as well as all participating families for sharing their perceptions and experiences with us.
The study was funded by the Doctoral Dissertation Fund of the Faculty of Medicine of the University Medical Center Hamburg-Eppendorf.
All authors have identified they have no financial relationships relevant to this study and its results to disclose.
Ethics approval and consent to participate
The study was approved by the Ethical Review Board of Magdeburg, Germany (45/15). All patients gave their informed consent to participate in the study.
Consent for publication
The authors declare that they have no competing interests.
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