Brachydactyly E: isolated or as a feature of a syndrome
© Pereda et al.; licensee BioMed Central Ltd. 2013
Received: 10 May 2013
Accepted: 3 September 2013
Published: 12 September 2013
Brachydactyly (BD) refers to the shortening of the hands, feet or both. There are different types of BD; among them, type E (BDE) is a rare type that can present as an isolated feature or as part of more complex syndromes, such as: pseudohypopthyroidism (PHP), hypertension with BD or Bilginturan BD (HTNB), BD with mental retardation (BDMR) or BDE with short stature, PTHLH type. Each syndrome has characteristic patterns of skeletal involvement. However, brachydactyly is not a constant feature and shows a high degree of phenotypic variability. In addition, there are other syndromes that can be misdiagnosed as brachydactyly type E, some of which will also be discussed. The objective of this review is to describe some of the syndromes in which BDE is present, focusing on clinical, biochemical and genetic characteristics as features of differential diagnoses, with the aim of establishing an algorithm for their differential diagnosis. As in our experience many of these patients are recruited at Endocrinology and/or Pediatric Endocrinology Services due to their short stature, we have focused the algorithm in those steps that could mainly help these professionals.
Brachydactyly (BD) refers to a family of limb malformations characterized by shortening of the hands, feet or both . It was added to the international Nosology and Classification of Genetic Skeletal Disorders in 2001, in the group of genetically determined dysostoses [2, 3]. Different types of brachydactyly can be distinguished based on anatomic grounds, the most commonly used classification being that provided by Bell  and modified by Temtamy & McKusick . Most types are rare, except for A3 (BDA3, OMIM#112700) and D (BDD, OMIM#113200) that have a prevalence of around 2% . In this review, we focus on brachydactyly type E (BDE, OMIM#113300), which is rare and can be diagnosed as an isolated finding or as part of several genetic syndromes [1, 5, 6].
BDE encompasses variable shortening of the metacarpals/metatarsals, frequently with involvement of the phalanges . Hertzog  classified BDE into three distinct varieties: type E1, with shortening of metacarpal IV, sometimes associated with shortening of metatarsal IV (possible involvement of an isolated metatarsal); type E2, with shortening of metacarpals IV and V (and metatarsals) associated with shortening of the distal phalanx of the thumb; and type E3, with various combinations of short metacarpals without phalangeal involvement . However, these patterns are not held to exactly in all syndromes; as well as the distal phalanx of the thumb, others phalanges are often shortened.
In this review, we describe some common syndromes in which BDE is present, outlining their main clinical, biochemical and genetic characteristics (Additional file 1: Table S1), with the aim of establishing an algorithm for the accurate diagnosis of BDE in association with other features. Even if acrodysostosis and tricho-rinho-phalangeal syndrome cannot be considered as conditions with a pure brachydactyly E, as they have peculiar radiological features, sometimes they are misdiagnosed as syndromic BDE, so we will try to define the specific characteristics that distinguish them from all the other conditions.
One of these specific features is multihormonal resistance, mainly to pthyroid hormone (PTH) and thyroid hormone (TSH). We use this feature to classify the syndromes into two groups depending on the presence of multihormonal resistance as many of these patients are recruited at Endocrinology and/or Pediatric Endocrinology Services due to their short stature that leads to the analysis of hormonal profile.
Isolated brachydactyly type E: HOXD13 type (OMIM#113300)
While BDE is commonly reported as part of a syndrome, it occasionally appears as an isolated entity [9–11]. Four heterozygous mutations in the homeobox D13 gene (HOXD13, 2q31.1), two missenses and two nonsenses, have been identified as causative of isolated BDE [9–12]. In two of these four cases, an overlap between BDE and BDD (shortening of the distal phalanx of the thumb) was noted in the patients . Other hand malformations that have been observed in combination with BDE are syndactyly of digits III and IV, synpolydactyly of finger IV, and long distal phalanges . In addition, 21 independent mutations have been identified in HOXD13, most of them producing synpolydactyly (SPD; OMIM#186000), or in rare cases syndactyly, and other unspecified limb malformations .
Brachydactyly type E as part of syndromes
BDE with multihormonal resistance
Pseudohypopthyroidism (PHP) refers to several distinct, but related, disorders in which resistance to pthyroid hormone (PTH) is the most prominent feature . However, resistance to thyroid-stimulating hormone (TSH) and several other pituitary hormones that mediate their action through G-protein-coupled receptors is often present as well. As a result of PTH resistance, patients with PHP develop hypocalcaemia and hyperphosphataemia. Resistance seems to occur only in the proximal renal tubule, while the action of PTH is unimpaired in other target tissues, such as bone and the renal thick ascending limb [16–18].
PHP is associated with alterations in the GNAS locus, which maps to the telomeric end of the long arm of chromosome 20 (20q13.2-20q13.3) . GNAS exemplifies a locus of high complexity . One of its products is the α-subunit of the stimulatory heterotrimeric G protein (Gsα), a ubiquitous signalling protein that is essential for numerous different cellular responses. Gsα expression is biallelic in most tissues, but paternal Gsα expression is silenced in a few types of tissue (renal tubule, thyroid gland, hypophysis and gonads) [24–26] and this is important in the development of phenotypes associated with GNAS mutations. Maternal imprinting (and thus paternal expression) occurs on XLαs, the large form of Gsα, and two non-coding RNA molecules, the A/B transcript and the NESPas antisense transcript. On the other hand, paternal imprinting is seen on NESP55, a chromogranin like neuroendocrine secretory protein .
Heterozygous inactivating mutations within Gsα-encoding GNAS exons, leading to diminished activity, are found in patients with PHP-Ia (OMIM#103580). These patients have not only resistance to hormones but also the Albright’s hereditary osteodystrophy (AHO) phenotype (as an example, see Figure one at Miao et al. ) (Additional file 1: Table S3) . This phenotype includes BDE (Figure 2), small stature, obesity with a rounded face, subcutaneous calcifications, and mental retardation . Patients with AHO features but no evidence of hormone resistance are said to have pseudopseudohypopthyroidism (PPHP, OMIM#612463), and also carry heterozygous inactivating Gsα mutations. Maternal inheritance of such a mutation leads to PHP-Ia, AHO and hormone resistance, while paternal inheritance of the same mutation causes PPHP .
On the other hand, PHP-Ib (OMIM#603233) is another form of PHP which can follow an autosomal dominant (AD) trait (AD-PHP-Ib) or occur as a sporadic disorder. These patients present with PTH and sometimes TSH resistance, but resistance for other hormones is not found. Apart from this, patients often lack AHO features and exhibit normal Gsα activity in erythrocytes and fibroblasts. Nevertheless, there have been some reports of patients with mild AHO [30–33] and these individuals have diminished Gsa activity . Generally, AD-PHP-Ib is caused by specific deletions in the syntaxin 16 gene (STX16) (STX16del4-6 or STX16del2-4); which are associated with maternal inheritance and cause loss of methylation at GNAS exon A/B or 1A. Other form of AD-PHP-Ib, due to maternally inherited microdeletions of NESP55 identified within GNAS, produces a loss of all maternal GNAS methylation imprints [35, 36].
Sporadic PHP-Ib cases also display GNAS imprinting abnormalities that involve NESPas, XLαs and A/B. However, the genetic lesion, if any, underlying these epigenetic defects remains to be discovered and most of these cases could represent true stochastic errors in early embryonic maintenance of methylation [37–39]. Some of these patients have been shown to be affected by paternal uniparental isodisomy (pat20iUPD) involving part or the whole long arm of chromosome 20, which includes the GNAS locus [39–42]. A mild BDE and AHO phenotype has been reported in some studies [30, 31, 43]; in most cases, only metacarpal IV and/or V shortening was seen, although mild shortening of all metacarpals and some distal phalanges has also been described . Sanchez et al. found BDE in 60% of patients with PHP-Ib in their study (no subjects presenting shortening of distal phalanx I). In two patients, BDE was combined with Madelung-like deformities (involvement of the distal ulna and radius) . On the other hand, Mantovani et al. did not find any correlation between the severity of the AHO phenotype and methylation defects, their patients’ phenotype ranging from mild to severe AHO .
Acrodysostosis with multihormonal resistance (ACRDYS1, OMIM#101800)
pthyroid hormone-related protein and G-proteins are part of the same signalling pathway affecting cartilage differentiation and growth in the metacarpals. This could explain the similarity of PTHLH-related BDE, pseudohypopthyroidism and acrodysostosis.
BDE without multihormonal resistance
Bilginturan BD or hypertension with brachydactyly syndrome (HTNB, OMIM%112410)
Bilginturan et al. were the first to describe this syndrome in a large non-consanguineous Turkish family . Subsequently, other authors have also studied this family and its new generations [55–66]. Affected members of the family had severe hypertension (30 mm Hg difference between affected and unaffected family members) from childhood  and a stroke by the age of 50 years if untreated . Almost all the affected children have systolic blood pressure values over the 99th percentile . However, the renin-angiotensin-aldosterone system (supine and upright) and circulating catecholamines respond normally, patients were not salt sensitive, their renal function was normal, they had no retinopathy or cardiac enlargement and the increase in radial wall thickness was minimal [55, 56, 59]. Affected individuals also presented BDE, were on average 10 cm shorter and had lower mean birth weight than their unaffected relatives, as well as having a stocky build and rather round face (see Figures two a & three a at Bilginturan et al. ) (Additional file 1: Table S5) [54, 56, 66].
Brachydactyly among the affected Turkish family members was heterogeneous. In most cases, shortening of more than one metacarpal and metatarsal was present , digits IV and V being most frequently affected but, in some cases, shortening has been seen in all the metacarpals and metatarsals in this and other families [56, 57, 66, 67]. Further, the shortening is not always symmetrical. All the phalanges of the hand were shortened, but the proximal and middle phalanges of the III and IV digits were relatively normal. Phalanges revealed cone-shaped epiphyses at proximal ends. All the phalanges of the toes were shortened and some patients presented symmetrical fusion between the middle and distal phalanges of toes IV and V, or only V (Figure 4). Additionally, shortening of carpal bones in the axial direction was also observed . Bähring et al. compared the brachydactyly pattern profile of a 5.5-year-old Japanese patient, who carried a de novo (12) (p11.21p12.2) chromosomal deletion , with a 6-year-old boy from the Turkish family . Both boys presented almost identical brachydactylies; type 16 cone-shaped epiphyses, particularly in the proximal interpahalangeal joints of digits II and V, brachyphalangy of digits II-IV and brachymetacarpalia of digits IV and V. The Japanese patient presented brachymesophalangy and cone-shaped epiphyses in digits II-V, and the Turkish boy only in digits II and V . Intellectual disability, subcutaneous calcifications, obesity or differences in body mass index have not been observed [55, 57, 66], except in an isolated case reported by Derbent et al., where the patient presented obesity and a defect in the left renal artery . It is important to highlight that brachydactyly is not appreciable until around 6 years of age and it aggravates significantly during early puberty as a result of an impaired growth spurt at the prepubertal stage. Given this, it is important to pay attention to the first signs of brachydactyly when an elevated blood pressure is detected in children (systolic blood pressure values >99th percentile) .
Another clinical feature in the Turkish family was the presence of aberrant posterior inferior cerebellar artery (PICA) loops only in affected members. Naraghi et al. reported 100% loop cosegregation with hypertension and brachydactyly in a group of 27 members of the Turkish family (15 affected and 12 unaffected). The prevalence of the loops was not influenced by age or sex. Further, a brief report described a case of a boy with the same syndrome not only with the PICA abnormality but also abnormal renal arteries . Additional studies found that affected individuals showed less active sympathetic nerve traffic to muscle than unaffected family members and also could not buffer blood pressure-elevating effects of phenylephrine [60, 65]. These findings confirmed that baroreflex blood pressure buffering was impaired in affected individuals [60, 66]. The arterial baroreflex is a critical cardiovascular reflex that provides continuous buffering of acute fluctuations in arterial blood pressure due, for example, to changes in posture, exercise, and emotion . PICA loops can produce neurovascular compression of the ventrolateral medulla at the root entry zone of cranial nerves IX and X [63, 70], which are very important in the baroreflex mechanism. Arterial baroreceptors are mechanoreceptors: those located in the carotid sinuses are innervated by cranial nerve IX and those in the aortic arch by cranial nerve X. When arterial pressure increases, these nerves send an input to the nucleus of the solitary tract and barosensitive neurons from here initiate a sympatho-inhibitory pathway to reduce arterial blood pressure .
The molecular basis for this syndrome is unknown, but several researchers have found evidence of linkage to chromosome 12p, specifically to 12p11.21-12p.12.2 [55, 56, 73, 74]. Surprisingly, in a genome-wide linkage analysis, chromosome 12p was also implicated in Chinese patients with primary hypertension (not brachydactyly) . Bahring et al. identified a complex rearrangement involving a deletion, reinsertion and inversion of the 12p12.2-p12.1 region . This region is, however, relatively gene poor, only further characterized expressed sequence tags (EST) being identified in the vicinity . These authors also proposed Kir6.1, SUR2, LSOX5 and PDE3A, which are within the studied segment, as candidate genes. Although, no alterations were found in these genes, a higher mRNA expression of PDE3A was detected in older affected family members (while the younger subjects affected showed expression values in the same range as those unaffected). On this basis, they suggested that the higher vascular expression of PDE3A was probably not the cause of the hypertension, but rather the result of an increase in blood pressure with age . Slightly different rearrangements in this segment were found later in other families, apart from the Turkish one . Finally, in this inverted sequence, a non-protein coding exon was found only to be expressed in unaffected family members; the rearrangement could be the cause for this lack of expression. This transcript was predicted to be an miRNA expressed in primary fibroblasts . The fibroblasts of affected family members showed faster cell growth, but the function of this miRNA remains to be clarified .
More severe cases caused by deletions in the 12p11.21-12p.12.2 region were reported by Lu et al. and Nagai et al.. One patient, with a deletion spanning 71 annotated genes (PDE3A→BICD1), had moderate mental retardation, short stature, borderline high blood pressure (120/80 mmHg) and characteristic brachydactyly . Another patient presented a more severe phenotype, mild mental retardation, short stature, high blood pressure, brachydactyly and cone-shaped epiphyses of the hands, hypoplastic hair and skin, oligodontia, a small thoracic cage and a hypoplastic pelvis . The difference in the severity between the patients might be attributable to the extent of the deletion .
BDE with short stature, PTHLH type (OMIM#613382)
Maass et al. were the first to implicate the pthyroid hormone-like hormone gene (PTHLH), localized to 12p11.22, in BDE, after the identification of a translocation, t(8;12) (q13;p11.2) in a family with autosomal-dominant BDE and other malformations, including short extremities, dysmorphic facies, macrocephaly, prominent forehead and a depressed nasal root . Despite the PTHLH gene not being disrupted by the translocation, it produced a downregulation of the gene and consequently of its downstream targets, ADAMTS-7 and ADAMTS-12. These genes are highly expressed in chondrogenically differentiated fibroblasts, so they seem to play an important role in chondrogenesis [77, 78]. In a more recent publication, Maass et al. proposed that the downregulation of PTHLH, and its targets, was due to the disruption of the interaction with a regulatory element localized 24.43 Mb downstream of PTHLH, CISTR-ACT. This element is a cis-regulatory element of PTHLH and also a trans-regulatory element of SOX9 (17q) [76, 80], which is another essential gene in chondrogenesis whose haploinsufficiency causes skeletal malformations . This regulation occurs by an lncRNA (DA125942), derived from the CISTR-ACT locus, that coordinates the expression of SOX9 and PTHLH generating a loop in the chromatin [79, 80]. The translocations t(8;12) (q13;p11.2) and t(4;12) (q13.2-13.3;p11.2), later identified in another family, prevent the formation of such a loop and result in overexpression of the lncRNA and misexpression of PTHLH and SOX9[79, 80].
In an independent study, a deletion and three point mutations in the coding sequence of PTHLH were found to be responsible for BDE with short stature . Further, in an isolated case of symmetrical enchondromatosis caused by a de novo duplication of 12p11.23 to 12p11.22 including PTHLH, the patient showed BDE with cone-shaped phalangeal epiphyses .
Apart from BDE, other features were seen in these patients (Additional file 1: Table S6): most but not all had short stature [76, 82], tooth problems were reported by Klopocki et al. in two out of five families , and those affected with translocation t(8;12) had dysmorphic facies with macrocephaly . Neither hypertension nor mental retardation was mentioned, but learning difficulties were reported in one family .
Brachydactyly mental retardation syndrome (BDMR, OMIM#600430)
Brachydactyly mental retardation syndrome (BDMR), also referred to as Albright hereditary osteodystrophy-like syndrome, is a rare pathology characterized by variable features: short stature, obesity, developmental delay, behavioural disorders, autism spectrum disorder and craniofacial and skeletal abnormalities, like BDE (see Figure one at Fernandez-Rebollo et al. ). Major malformations have also been reported, including cardiac, tracheal, gastrointestinal, genitourinary, CNS and skeletal abnormalities (Additional file 1: Table S7) [85, 86].
This syndrome is caused by deletions in 2q37. Recently, the minimum critical region responsible for this syndrome has been mapped to the 200 kb which involve the histone deacetylase 4 gene (HDAC4), localized exactly to 2q37.3 . In addition, point mutations in HDAC4 have been found in two patients with BDMR . On the other hand, a patient with a deletion in 2q37.3, but not including HDAC4, exhibited a similar phenotype but without BDE, cardiac or other major malformations . Given this, it was proposed that HDAC4 haploinsufficiency could be causative of BDE in this syndrome . A recent report, of a family case with a microdeletion involving HDAC4 and other two genes, puts this statement in doubt, because none of the three affected patients showed BDE . So far, we know that BDE is a variable feature and only reported in about a half of patients with 2q37 microdeletions .
Histone deacetylase 4 is involved in bone, muscle, neurological and cardiac development . Felder et al. demonstrated that FARP2, HDLBP and PASK genes were downregulated in a patient with a 2q37.3 terminal deletion compared to levels in his healthy family members and controls . These are good candidate genes because they are involved in neuronal and/or skeletal development , but point mutations in these genes which cause BDMR or other similar syndrome have not yet been reported in the bibliography, except for the case of a patient with autism associated with a de novo MECP2 duplication who also had a second de novo duplication of 2q37.3 material involving PASK and HDLBP. However, this patient did not have an AHO-like phenotype .
BDE is only penetrant in 50-60% of cases and the pattern profile is variable [88, 92]. Frequently, metacarpals III and IV and metatarsal IV are shortened, but other metacarpals (II-V) have also been found to be affected, generally sparing metacarpal/metatarsal I [86, 88, 90, 93–98]. Further, individuals with similar deletions or family members with the same deletion may present different phenotypes; this could be a result of incomplete penetrance of the haploinsufficiency genes, epigenetics or regulation by other genes .
It is worth mentioning that there is a very similar syndrome, but without BDE, known as Smith-Magenis syndrome (SMS; OMIM#182290) which is caused by deletions in 17p11.2 or mutations in the RAI1 gene . In addition, RAI1 expression is reduced in BDMR cases . Hence, when individuals are suspected of having the BDMR phenotype, but no 2q37 deletions or HDAC4 mutations are detected, deletions at 17p11.2 and the RAI1 gene should be analysed.
Acrodysostosis without multihormonal resistance (ACRDYS2, OMIM:#614613)
In acrodysostosis without hormonal resistance, the affected gene is the phosphodiesterase 4D, cAMP-specific (PDE4D) gene, localized to 5q11.2 [44, 46, 49, 99]. Clinical features (Additional file 1: Table S4) are similar to ACRDYS1 apart from PTH resistance not generally being present [44, 99], though an exception was reported by Michot et al.. Other features it has been suggested may differ in the two types are: (i) facial dysostosis, which is more evident in ACRDYS2 than in ACRDYS1; and (ii) intellectual disability, which is common in ACRDYS2, while ACRDYS1 has only been associated with some behavioural disorders and/or learning difficulties [44, 46]. On the other hand, in the study of Lee et al. all patients (three with PDE4D and two with PRKAR1A mutations) had midface hypoplasia and there were no differences in developmental disability according to the gene affected (among those with PDE4D mutations, one was not affected, a second was mildly affected and a third was significantly affected; whereas both patients with PRKAR1A mutations had mild developmental disabilities) . Lynch et al. described eight patients; all of them had some degree of learning difficulties, developmental delay and intellectual disability . These authors suggested that in patients with acrodysostosis associated with normal stature (only 5/15 presented short stature [46, 49, 99]), progressive obesity (frequently developing after 6 years of age), and mild intellectual disability but no PTH resistance, PDE4D rather than PRKAR1A mutations should be suspected. BDE, stenosis of the lumbar spine, nasal hypoplasia, a flat nasal bridge and short stature are features shared by both subtypes of acrodysostosis (see Figure three Pat. 15, 16 at Linglart et al. ). In addition, some cases of hypogonadism have been found with defects in either gene [44, 49, 99].
Thus, it is difficult to distinguish acrodysostosis cases with PDE4D mutations from those with PRKAR1A mutations on the basis of clinical observation only . Therefore, biochemical studies of calcium and phosphorus metabolism are essential.
Tricho-rhino-phalangeal syndrome (TRPS)
This syndrome is classified into three types: TRPS I (OMIM#190350), TRPS II (OMIM#150230) and TRPS III (OMIM#190351). Mutations in the trichorhinophalangeal syndrome I gene (TRPS1), localized to 8q23.3, have been found in 88% of cases of TRSP I and TRSP III . Lüdecke et al. described TRPS III as an extreme of the clinical spectrum of TRSP I . On the other hand, TRPS II is a contiguous gene syndrome involving TRPS1 and EXT1 genes; patients develop cartilaginous exostoses in addition to the features seen in TRPS I and III [100, 101].
The striking features shared by the three types are sparse, slowly growing scalp hair, laterally sparse eyebrows, a bulbous tip of the nose (pear-shaped nose), long flat philtrum, thin upper vermillion border and protruding ears (see Figure three Momeni et al. ) (Additional file 1: Table S8) . In radiography, the main findings are: short stature, BDE, mild metaphyseal convexity during the first year of life and premature fusion of the growth plates of the tubular bonds . Additionally, hip malformations (coxa plana, coxa magna or coxa vara) have been reported in more than 70% of cases and degenerative arthrosis appears in older individuals . Patients show a retarded skeletal age until puberty, and then an accelerated skeletal age, while the mean length at birth is normal . That is, the growth retardation is a progressive process that can be appreciated in metacarpophalangeal pattern profile (MCPP) analysis comparing children and adults, and comparisons of their relative height . Growth hormone deficiency has been reported in some cases [103–105]. Intellectual disability has also been reported in the three types, but most commonly in TRPS II [100, 101, 106, 107].
The severity of the TRPS phenotype might also depend on the size of the deletion in 8q and whether there is mosaicism for the deletion, which has been reported in four patients, two with TRPS I and two with TRPS II .
Turner syndrome (TS)
Turner syndrome is a chromosomal disorder with a complete or partial monosomy of X chromosome. The genetic background is variable, the most frequent karyotypes are: 45,X (~50%), karyotypes with an isochromosome of X (i(Xq) or i(Xp)), the mosaic 45,X/46XX (%30), and karyotypes containing an entire or parts of Y chromosome [111, 112].
The main features are short stature (90-100%), gonadal dysgenesis, pubertal delay, primary amenorrhea (85%), estrogens insufficiency, cardiac anomalies and/or other congenital malformations like brachydactyly E (see Figure one at Bondy ) [111, 112, 114–116]. Other frequent features are: lymphedema, congenital malformations of the urinary system (30-40%), abnormalities of the external ocular appendages, (epicanthal folds, ptosis, hypertelorism, upward slanting palpebral fissures), strabismus and hypermetropia (25–35%), hearing problems and ear malformations, dysmorphic craniofacial features, abnormalities in tooth development and morphology (early eruption), melanocytic nevi, normal GH secretory pattern, altered liver enzymes¸ decreased bone mineral density, etc. [111, 112, 114–117] (Additional file 1: Table S9).
Although TS is quite well known entity, there is often a delay in the diagnosis as over 20% of patients are diagnosed after 12 yr [115, 119]. As other syndromes mentioned in this review, it is essential to be diagnosed during infancy for proper early treatment to avoid complications linked to TS. In fact there are some publications explaining the clinical guidelines to be followed to optimize care for young woman and adults with TS [111, 112, 114–117].
The BDE pattern profile can vary considerably within a syndrome, even between unrelated patients with identical mutations and among affected family members. In addition, brachydactyly is sometimes not appreciable until 6 years of age, because it is a progressive feature and tends to become more evident during early puberty.
Poznanski et al. also carried out MCPP analysis comparing isolated BDE and PHP/PPHP, but at the time these two syndromes had not been genetically well differentiated and hence the conclusions may not be reliable . Indeed, patients with different pathologies could be confused if attention were to be focused on radiographic findings alone; hence, biochemical analyses should be included.
The other syndromes discussed have not yet been compared by MCPP analysis, but it seems that the pattern of brachydactyly does not differ appreciably between them. In such cases, when the BDE pattern is not sufficiently informative, there are other features which can help in the differentiation of each syndrome (Additional file 1: Table S1). These features are listed in the supplementary material (Additional file 1: Table S2–S9).
We thank all the members of the Spanish PHP group for their clinical advice and all the people that provide us with clinical radiographies to complete our review: Dr. Aleksander Jamsheer, Prof. Dr. Jesus Argente, Dr. Beatriz Garcia-Cuartero, Dr. Sylvia Bähring, Dr. Okan Toka, Dr. Cécile Teinturier-Thomas, Dr. Caroline Silve and Dr. Sharona Azriel.
This work was partially supported by the Carlos III Health Institute (PI10/0148). Mrs Arrate Pereda is funded by the Spanish Ministry of Health (FI11/00309), Dr Intza Garin by a Spanish fund for health research (FIS) programme (I3SNSCA10/01056), Dr Elena Beristain by a grant from the Spanish Ministry of Science and Innovation (MICINN; PTA2009-2147), and Dr Guiomar Perez de Nanclares in part by the I3SNS Programme of the Spanish Ministry of Health (CP03/0064; SIVI 1395/09).
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