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Syndromic (phenotypic) diarrhea in early infancy
© Goulet et al; licensee BioMed Central Ltd. 2008
Received: 19 July 2007
Accepted: 28 February 2008
Published: 28 February 2008
: Syndromic diarrhea (SD), also known as phenotypic diarrhea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhea requiring parenteral nutrition (PN). To date, no epidemiological data are available. The estimated prevalence is approximately 1/300,000–400,000 live births in Western Europe. Ethnic origin does not appear to be associated with SD. Infants are born small for gestational age and present with facial dysmorphism including prominent forehead and cheeks, broad nasal root and hypertelorism. Hairs are woolly, easily removed and poorly pigmented. Severe and persistent diarrhea starts within the first 6 months of life (≤ 1 month in most cases) and is accompanied by severe malabsorption leading to early and relentless protein energy malnutrition with failure to thrive. Liver disease affects about half of patients with extensive fibrosis or cirrhosis. There is currently no specific biochemical profile, though a functional T-cell immune deficiency with defective antibody production was reported. Microscopic analysis of the hair show twisted hair (pili torti), aniso- and poilkilotrichosis, and trichorrhexis nodosa. Histopathological analysis of small intestine biopsy shows non-specific villous atrophy with low or no mononuclear cell infiltration of the lamina propria, and no specific histological abnormalities involving the epithelium. The etiology remains unknown. The frequent association of the disorder with parental consanguinity and/or affected siblings suggests a genetic origin with an autosomal recessive mode of transmission. Early management consists of total PN. Some infants have a rather milder phenotype with partial PN dependency or require only enteral feeding. Prognosis of this syndrome is poor, but most patients now survive, and about half of the patients may be weaned from PN at adolescence, but experience failure to thrive and final short stature.
Disease name and synonyms
Syndromic diarrhea – Phenotypic diarrhea – Tricho-hepato-enteric syndrome – Intractable diarrhea of infancy with facial dysmorphism – Trichorrhexis nodosa and cirrhosis – Neonatal hemochromatosis phenotype with intractable diarrhea and hair abnormalities – Intractable infant diarrhea associated with phenotypic abnormalities and immune deficiency.
To date, several types of early onset intractable diarrhea of infancy (IDI) have been recognized [1–8]. Some of them involve primary epithelial abnormalities such as microvillous atrophy also called microvillous inclusion disease  and, more recently, intestinal epithelial dysplasia also called tufting enteropathy [6, 7], while others are related to autoimmune disorders or complex syndromes involving mitochondrial disease or glycosylation proteins. The so-called "syndromic diarrhea" is an IDI syndrome associated with phenotypic abnormalities .
Syndromic diarrhea (SD), also known as Phenotypic diarrhea (PD) or Tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset severe intractable diarrhea in infants born Small for Gestational Age (SGA) and associated with non-specific villous atrophy with low or no mononuclear cell infiltration of the lamina propria nor specific histological abnormalities involving the epithelium. The diarrhea is associated with facial dysmorphism, immune disorders and, in some patients, early onset of severe liver cirrhosis.
History of the description
SD is a newly described clinicopathologic entity with intractable diarrhea in infants. Two cases have been reported by Stankler et al. as unexplained diarrhea and failure to thrive in two siblings with unusual facies and abnormal scalp hair shafts . To date, the largest series involving 8 cases presenting a syndrome of intractable diarrhea associating phenotypic abnormalities and immune deficiency has been reported by Girault D et al. in 1994 . Further case reports have confirmed the existence of the new entity [11–15]. Some cases reported by Girault D et al.,1994 presented with an early-onset severe cholestatic disease that rapidly progressed to cirrhosis and death . A recent report (including two cases with severe liver disease) and the review of the published cases suggested that these patients have the same heterogeneous disease (inappropriately separated into different entities), suggesting that SD and THE are two sides of a now well recognized disease of unclear origin .
SD appears to be much less common than microvillous atrophy [5, 7] or intestinal epithelial dysplasia [6, 8]. Many cases are not yet recognized since the description of this disorder is recent. To date, no epidemiological data are available. However, the prevalence can be estimated at around 1/300,000–400,000 live births in Western Europe. The largest cohort of patients has been reported at the Necker-Enfants Malades Hospital in Paris, France . The prevalence does not seem to differ significantly between ethnic groups. The disease seems to be more common in regions with a higher degree of consanguinity.
In patients presenting with liver disease, pathological analysis of the liver usually shows macronodular cirrhosis with normal extra-hepatic ducts. Light microscopy examination shows extensive fibrosis or cirrhosis. Perl's staining shows iron depositions involving the hepatocytes and, to a lesser extent, the Kupfer cells. This aspect is consistent with neonatal hemochromatosis as suggested by Verloes et al. .
Published profiles have been studied by performing a complete immunologic work-up, including analysis of the T- and B- cell populations, and mitogen (PHA, concavaline A, PWM), antigen (Candida albicans, tetanus toxoid) and allogenic cell-induced lymphocyte proliferation. Serum immunoglobulin levels and specific antibody titers to poliovirus, tetanus, Diphteria toxoid and Bordetella pertussis were also measured in most reports. Functional T-cell immune deficiency with defective antibody production was described in the original report . Patients had defective antibody responses despite normal serum immunoglobulin levels, and defective antigen-specific skin tests despite positive proliferative responses in vitro. Further reports, in which extensive immunologic work-ups have been done, confirmed immune dysfunction. Several cases presented with monoclonal hyper IgA and/or hypo IgG [9, 12]. The search for an abnormal immune profile and immune dysfunction should be part of the diagnosis work-up in the case of suspected SD.
Among the congenital forms of hair dysplasia, tricorrhexis nodosa (TN) is very common and can be present in several pathologic conditions [16–19]. TN is the most common defect in the hair shaft, leading to hair breakage . The primary abnormality is a focal loss of cuticles, causing fraying of the cortical fibers [21, 22]. As emphasized by Landers et al., TN may occur congenitally or can be acquired from chemical or physical trauma. Congenital TN has been associated with several syndromes including arginosuccinaciduria , citrullinemia [24, 25], Menkes syndrome , Netherton disease [27, 28], and syndromes associated with trichothiodystrophy hair shaft defect . SD patients have defective antibody responses despite normal serum immunoglobulin levels, and defective antigen-specific skin tests despite positive proliferative responses in vitro. The cause of this functional immune deficiency and of this severe protracted diarrhea is unknown. The relationship between low birth weight, dysmorphism, severe diarrhea, hair shaft defect, immune deficiency and neonatal hemochromatosis-like liver disease is unclear. The coexistence of morphological, trichological and immunological abnormalities with early-onset intractable diarrhea disproportionate to the mucosal architectural abnormality (consistent with a primary enterocyte abnormality) suggests either mutations within several genes, inherited together by linkage disequilibrium, or, more probably, interference with a higher level of control, such as a patterning gene as seen in the Netherton syndrome which is an autosomal recessive congenital ichthyosis featuring chronic inflammation of the skin, hair anomalies, epidermal hyperplasia with an impaired epidermal barrier function, failure to thrive and atopic manifestations. The disease is caused by mutations in the SPINK5 gene encoding the serine proteinase inhibitor lympho-epithelial Kazal-type inhibitor [30, 31]. The characteristic hair abnormalities may allow a more focused search for candidate mutations, as relatively few genes have been implicated in hair development.
Mode of transmission
The frequent association of the disorder with parental consanguinity and/or affected siblings suggests a genetic origin with an autosomal recessive transmission [Additional file 1]. The gene involved in this congenital inherited disease has not yet been identified. Ethnic origin does not appear to be associated with the disease. Extensive case reports and specimen collection should allow future genetic studies to be performed.
intra-uterine growth retardation
severe protracted diarrhea of early onset
abnormal face with prominent forehead and cheeks
Most patients also have abnormal hair with tricorrhexis nodosa, immune deficiency, long-term growth failure and mental retardation in common. Liver disease is associated in about half of the patients and is variable in severity.
Management and outcome
Early management consists of total parenteral nutrition (TPN) using central venous catheter in an experienced clinical setting. Patients usually have persistent diarrhea and, in enterally fed patients, malabsorption is severe. Its mechanisms are unknown, as villous atrophy is usually not as severe as the diarrhea is, and small bowel bacterial overgrowth or specific malabsorption have never been documented in these patients. Long-term PN is required for achieving growth even if catch up growth, in patients born SGA, cannot be achieved. Attempts at enteral feeding should be performed in all cases using semi-elemental diet or amino-acid formulas. Some patients will tolerate progressive increase of enteral feeding making them able to be weaned from PN. However, normal growth velocity is not always achieved on full enteral feeding. Course may vary according to the concomitant liver disease, the severity of the digestive disease and the occurrence of infections. It is well reflected by the reported cases [Additional file 1]. It is important to note that the liver disease is, in some cases, already present at onset of diarrhea and before diagnosis is established. In these cases, the liver disease is due to the disease rather than to the PN, suggesting that the PN should be carefully adapted according to the liver disease. Indeed, the associated liver disease may be worsened by a long-term inappropriate PN (continuous PN, lipid free, complicated by infections etc.) with rapid course to end-stage liver disease and patient death.
Finally, the prognosis of this type of intractable diarrhea of infancy is poor, with >25% of the currently reported patients who died between the ages of 2 and 5 years, some of them with early onset of cirrhosis. In the largest but oldest series, five of the eight children reported died within 5 years due to sepsis or cirrhosis, despite aggressive intervention . More recent case reports described better survival with long-term PN dependency or PN weaning in some cases [11–15]. In many patients, the severity of intestinal malabsorption and diarrhea makes them dependent on a daily long-term PN with subsequent risk of complications. However, it seems that some infants have milder phenotype with partial PN dependency or require only enteral feeding. In spite of adequate protein energy supplies, growth velocity remains low and final stature very short [9, 11–14]. Attempts with recombinant human growth hormone was used in one patient (data unpublished), but failed to improve growth and final stature. Most of the reported patients have intellectual deficiency of variable severity. Some were too young when they died to be thoroughly evaluated.
This very rare and heterogeneous syndrome has a poor prognosis with early death, liver cirrhosis or failure to thrive, and short stature with intellectual deficiency in the survivors. The heterogeneity of SD as well as the very different associated symptoms makes it very difficult to find an approach for understanding the genetic origin of the disease.
Prognosis has improved since the description of the first case with SD. Most patients now survive and about half of the patients may be weaned from PN at adolescence, but experience failure to thrive and final short stature.
Written consent for publication of Figure 1 was obtained from the patient's parents.
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