Literature DB >> 17318842

Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorder.

Alexandre Fabre1, Nicolas André, Anne Breton, Pierre Broué, Catherine Badens, Bertrand Roquelaure.   

Abstract

Tricho-hepato-enteric syndrome and syndromic diarrhea are quite rare conditions with only 15 patients described to date. Both include severe diarrhea requiring total parenteral nutrition, facial dysmorphism, immunity defect, and hair abnormalities (mostly trichorrhexis nodosa). A definite clear clinical description of the two syndromes is lacking; the outcome is also poorly known. Here, we report on two additional patients. Analysis of our observations together with a review of previously published cases suggests that patients with tricho-hepato-enteric syndrome and/or syndromic diarrhea actually have the same heterogeneous disease that has been incorrectly and confusingly separated into different entities. The acknowledgment that these two syndromes represent the same disease is a crucial step toward a better description of this syndrome and its outcome toward studies of the underlying genetic cause. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17318842     DOI: 10.1002/ajmg.a.31634

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  11 in total

1.  SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome.

Authors:  Alexandre Fabre; Bernard Charroux; Christine Martinez-Vinson; Bertrand Roquelaure; Egritas Odul; Ersin Sayar; Hilary Smith; Virginie Colomb; Nicolas Andre; Jean-Pierre Hugot; Olivier Goulet; Caroline Lacoste; Jacques Sarles; Julien Royet; Nicolas Levy; Catherine Badens
Journal:  Am J Hum Genet       Date:  2012-03-22       Impact factor: 11.025

Review 2.  Management of syndromic diarrhea/tricho-hepato-enteric syndrome: A review of the literature.

Authors:  Alexandre Fabre; Patrice Bourgeois; Marie-Edith Coste; Céline Roman; Vincent Barlogis; Catherine Badens
Journal:  Intractable Rare Dis Res       Date:  2017-08

3.  Trichohepatoenteric syndrome: founder mutation in asian indians.

Authors:  U H Kotecha; S Movva; R D Puri; I C Verma
Journal:  Mol Syndromol       Date:  2012-07-05

4.  Tricho-hepato-enteric syndrome presenting with mild colitis.

Authors:  Odul Egritas; Buket Dalgic; Meltem Onder
Journal:  Eur J Pediatr       Date:  2008-11-04       Impact factor: 3.183

5.  Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric Syndrome.

Authors:  Nicholas L Rider; Bertrand Boisson; Soma Jyonouchi; Eric P Hanson; Sergio D Rosenzweig; Jean-Laurent Cassanova; Jordan S Orange
Journal:  Front Pediatr       Date:  2015-01-30       Impact factor: 3.418

6.  Exome sequencing identifies a novel TTC37 mutation in the first reported case of Trichohepatoenteric syndrome (THE-S) in South Africa.

Authors:  Craig Kinnear; Brigitte Glanzmann; Eric Banda; Nikola Schlechter; Glenda Durrheim; Annika Neethling; Etienne Nel; Mardelle Schoeman; Glynis Johnson; Paul D van Helden; Eileen G Hoal; Monika Esser; Michael Urban; Marlo Möller
Journal:  BMC Med Genet       Date:  2017-03-14       Impact factor: 2.103

7.  Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy).

Authors:  Jane Louise Hartley; Nicholas C Zachos; Ban Dawood; Mark Donowitz; Julia Forman; Rodney J Pollitt; Neil V Morgan; Louise Tee; Paul Gissen; Walter H A Kahr; Alex S Knisely; Steve Watson; David Chitayat; Ian W Booth; Sue Protheroe; Stephen Murphy; Esther de Vries; Deirdre A Kelly; Eamonn R Maher
Journal:  Gastroenterology       Date:  2010-02-20       Impact factor: 22.682

Review 8.  Syndromic diarrhea/Tricho-hepato-enteric syndrome.

Authors:  Alexandre Fabre; Christine Martinez-Vinson; Olivier Goulet; Catherine Badens
Journal:  Orphanet J Rare Dis       Date:  2013-01-09       Impact factor: 4.123

Review 9.  Syndromic (phenotypic) diarrhea in early infancy.

Authors:  Olivier Goulet; Christine Vinson; Bertrand Roquelaure; Nicole Brousse; Christine Bodemer; Jean-Pierre Cézard
Journal:  Orphanet J Rare Dis       Date:  2008-02-28       Impact factor: 4.123

10.  Identifying Mutations of the Tetratricopeptide Repeat Domain 37 (TTC37) Gene in Infants With Intractable Diarrhea and a Comparison of Asian and Non-Asian Phenotype and Genotype: A Global Case-report Study of a Well-Defined Syndrome With Immunodeficiency.

Authors:  Wen-I Lee; Jing-Long Huang; Chien-Chang Chen; Ju-Li Lin; Ren-Chin Wu; Tang-Her Jaing; Liang-Shiou Ou
Journal:  Medicine (Baltimore)       Date:  2016-03       Impact factor: 1.889

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