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Published in: European Journal of Pediatrics 10/2015

01-10-2015 | Case Report

Tricho-hepato-enteric syndrome (THE-S): two cases and review of the literature

Authors: Jin Ho Chong, Saumya Shekhar Jamuar, Christina Ong, Koh Cheng Thoon, Ee Shien Tan, Angeline Lai, Mark Koh Jean Aan, Wilson Lek Wen Tan, Roger Foo, Ene Choo Tan, Yu-Lung Lau, Woei Kang Liew

Published in: European Journal of Pediatrics | Issue 10/2015

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Abstract

Tricho-hepato-enteric syndrome (THE-S) is characterized by severe infantile diarrhea, failure to thrive, dysmorphism, woolly hair, and immune or hepatic dysfunction. We report two cases of East Asian descent with THE-S who had remained undiagnosed despite extensive investigations but were diagnosed on whole exome sequencing (WES). Both cases presented with chronic diarrhea, failure to thrive, and recurrent infections. Case 1 had posteriorly rotated low set ears, mild retrognathia, and fine curly hypopigmented hair. She was managed with prolonged total parenteral nutrition and intravenous immunoglobulin infusions. Case 2 had sparse coarse brown hair as well as multiple lentigines and café-au-lait macules. She was managed with amino acid-based formula. For both cases, routine investigations were inconclusive. WES in both cases showed biallelic truncating mutations in TTC37 (c.3507T>G;p.Y1169X and c.3601C>T;p.R1201X in case 1 and c.3507T>G;p.Y1169X and c.154G>T;p.E52X in case 2), suggesting a diagnosis of THE-S.
Conclusion: We present novel mutations in the TTC37 gene in two individuals of East Asian descent with the rare THE-S, detected by WES. Future identification of patients with THE-S and establishing genotype-phenotype correlations will aid in counseling the patients and their families.
What is Known:
Tricho-Hepato-Enteric syndrome (THE-S) is characterized by severe infantile diarrhea, failure to thrive, dysmorphism, woolly hair, and immune or hepatic dysfunction.
Complex patients with diagnostic dilemmas undergo extensive investigations.
What is New:
This is a report of novel mutations in TTC37 in individuals of East Asian descent.
Whole exome sequencing (WES) can be useful in certain complex cases with diagnostic dilemmas.
Literature
1.
go back to reference Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA (2012) An integrated map of genetic variation from 1,092 human genomes. Nature 491:56–65. doi:10.1038/nature11632 CrossRefPubMed Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA (2012) An integrated map of genetic variation from 1,092 human genomes. Nature 491:56–65. doi:10.​1038/​nature11632 CrossRefPubMed
3.
go back to reference DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, McKenna A, Fennell TJ, Kernytsky AM, Sivachenko AY, Cibulskis K, Gabriel SB, Altshuler D, Daly MJ (2011) A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 43:491–498. doi:10.1038/ng.806 PubMedCentralCrossRefPubMed DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, McKenna A, Fennell TJ, Kernytsky AM, Sivachenko AY, Cibulskis K, Gabriel SB, Altshuler D, Daly MJ (2011) A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 43:491–498. doi:10.​1038/​ng.​806 PubMedCentralCrossRefPubMed
6.
go back to reference Fabre A, Breton A, Coste ME, Colomb V, Dubern B, Lachaux A, Lemale J, Mancini J, Marinier E, Martinez-Vinson C, Peretti N, Perry A, Roquelaure B, Venaille A, Sarles J, Goulet O, Badens C (2014) Syndromic (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome. Arch Dis Child 99:35–38. doi:10.1136/archdischild-2013-304016 CrossRefPubMed Fabre A, Breton A, Coste ME, Colomb V, Dubern B, Lachaux A, Lemale J, Mancini J, Marinier E, Martinez-Vinson C, Peretti N, Perry A, Roquelaure B, Venaille A, Sarles J, Goulet O, Badens C (2014) Syndromic (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome. Arch Dis Child 99:35–38. doi:10.​1136/​archdischild-2013-304016 CrossRefPubMed
9.
go back to reference Kammermeier J, Drury S, James CT, Dziubak R, Ocaka L, Elawad M, Beales P, Lench N, Uhlig HH, Bacchelli C, Shah N (2014) Targeted gene panel sequencing in children with very early onset inflammatory bowel disease–evaluation and prospective analysis. J Med Genet 51:748–755. doi:10.1136/jmedgenet-2014-102624 CrossRefPubMed Kammermeier J, Drury S, James CT, Dziubak R, Ocaka L, Elawad M, Beales P, Lench N, Uhlig HH, Bacchelli C, Shah N (2014) Targeted gene panel sequencing in children with very early onset inflammatory bowel disease–evaluation and prospective analysis. J Med Genet 51:748–755. doi:10.​1136/​jmedgenet-2014-102624 CrossRefPubMed
13.
go back to reference Oz-Levi D, Weiss B, Lahad A, Greenberger S, Pode-Shakked B, Somech R, Olender T, Tatarsky P, Marek-Yagel D, Pras E, Anikster Y, Lancet D (2014) Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome. Clin Genet. doi:10.1111/cge.12494 PubMed Oz-Levi D, Weiss B, Lahad A, Greenberger S, Pode-Shakked B, Somech R, Olender T, Tatarsky P, Marek-Yagel D, Pras E, Anikster Y, Lancet D (2014) Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome. Clin Genet. doi:10.​1111/​cge.​12494 PubMed
14.
go back to reference Rider NL, Boisson B, Jyonouchi S, Hanson EP, Rosenzweig SD, Cassanova JL, Orange JS (2015) Novel TTC37 mutations in a patient with immunodeficiency without diarrhea: extending the phenotype of trichohepatoenteric syndrome. Front Pediatr 3:2. doi:10.3389/fped.2015.00002 PubMedCentralPubMed Rider NL, Boisson B, Jyonouchi S, Hanson EP, Rosenzweig SD, Cassanova JL, Orange JS (2015) Novel TTC37 mutations in a patient with immunodeficiency without diarrhea: extending the phenotype of trichohepatoenteric syndrome. Front Pediatr 3:2. doi:10.​3389/​fped.​2015.​00002 PubMedCentralPubMed
16.
go back to reference Sherry ST, Ward MH, Kholodov M, Baker J, Phan L, Smigielski EM, Sirotkin K (2001) dbSNP: the NCBI database of genetic variation. Nucleic Acids Res 29:308–311PubMedCentralCrossRefPubMed Sherry ST, Ward MH, Kholodov M, Baker J, Phan L, Smigielski EM, Sirotkin K (2001) dbSNP: the NCBI database of genetic variation. Nucleic Acids Res 29:308–311PubMedCentralCrossRefPubMed
17.
go back to reference Uhlig HH, Schwerd T, Koletzko S, Shah N, Kammermeier J, Elkadri A, Ouahed J, Wilson DC, Travis SP, Turner D, Klein C, Snapper SB, Muise AM (2014) The diagnostic approach to monogenic very early onset inflammatory bowel disease. Gastroenterology 147(990-1007), e1003. doi:10.1053/j.gastro.2014.07.023 Uhlig HH, Schwerd T, Koletzko S, Shah N, Kammermeier J, Elkadri A, Ouahed J, Wilson DC, Travis SP, Turner D, Klein C, Snapper SB, Muise AM (2014) The diagnostic approach to monogenic very early onset inflammatory bowel disease. Gastroenterology 147(990-1007), e1003. doi:10.​1053/​j.​gastro.​2014.​07.​023
19.
go back to reference Yang Y, Muzny DM, Reid JG, Bainbridge MN, Willis A, Ward PA, Braxton A, Beuten J, Xia F, Niu Z, Hardison M, Person R, Bekheirnia MR, Leduc MS, Kirby A, Pham P, Scull J, Wang M, Ding Y, Plon SE, Lupski JR, Beaudet AL, Gibbs RA, Eng CM (2013) Clinical whole-exome sequencing for the diagnosis of Mendelian disorders. N Engl J Med 369:1502–1511. doi:10.1056/NEJMoa1306555 PubMedCentralCrossRefPubMed Yang Y, Muzny DM, Reid JG, Bainbridge MN, Willis A, Ward PA, Braxton A, Beuten J, Xia F, Niu Z, Hardison M, Person R, Bekheirnia MR, Leduc MS, Kirby A, Pham P, Scull J, Wang M, Ding Y, Plon SE, Lupski JR, Beaudet AL, Gibbs RA, Eng CM (2013) Clinical whole-exome sequencing for the diagnosis of Mendelian disorders. N Engl J Med 369:1502–1511. doi:10.​1056/​NEJMoa1306555 PubMedCentralCrossRefPubMed
Metadata
Title
Tricho-hepato-enteric syndrome (THE-S): two cases and review of the literature
Authors
Jin Ho Chong
Saumya Shekhar Jamuar
Christina Ong
Koh Cheng Thoon
Ee Shien Tan
Angeline Lai
Mark Koh Jean Aan
Wilson Lek Wen Tan
Roger Foo
Ene Choo Tan
Yu-Lung Lau
Woei Kang Liew
Publication date
01-10-2015
Publisher
Springer Berlin Heidelberg
Published in
European Journal of Pediatrics / Issue 10/2015
Print ISSN: 0340-6199
Electronic ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-015-2563-z

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