Literature DB >> 28944135

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

Alexandre Fabre1,2, Patrice Bourgeois2,3, Marie-Edith Coste1, Céline Roman1, Vincent Barlogis4, Catherine Badens2,3.   

Abstract

Syndromic diarrhea/tricho-hepato-enteric syndrome (SD/THE) is a rare disease linked to the loss of function of either TTC37 or SKIV2L, two components of the SKI complex. It is characterized by a combination of 9 signs (intractable diarrhea, hair abnormalities, facial dysmorphism, immune abnormalities, IUGR/SGA, liver abnormalities, skin abnormalities, congenital heart defect and platelet abnormalities). We present a comprehensive review of the management of SD/THE and tested therapeutic regimens. A review of the literature was conducted in May 2017: 29 articles and 2 abstracts were included describing a total of 80 patients, of which 40 presented with mutations of TTC37, 14 of SKIV2L. Parenteral nutrition was used in the management of 83% of the patients and weaned in 44% (mean duration of 14.97 months). Immunoglobulins were used in 33 patients, but data on efficacy was reported for 6 patients with a diminution of infection (n = 3) or diarrhea reduction (n = 2). Antibiotics (n = 11) provided no efficacy. Steroids (n = 17) and immunosuppressant drugs (n = 13) were used with little efficacy and mostly in patients with IBD-like SD/THE. Hematopoietic stem cell transplantation (HSCT) was performed in 4 patients: 2 died, for one it corrected the immune defects but not the other features and for the last one, it provided only a partial improvement. Finally, no specific diet was effective except for some contradictory reports for elemental formula. In conclusion, the management of SD/THE mainly involves parenteral nutrition and immunoglobulin supplementation. Antibiotics, steroids, immunosuppressants, and HSCT are not recommended as principle treatments since there is no evidence of efficacy.

Entities:  

Keywords:  SKIV2L; TTC37; very early onset IBD

Year:  2017        PMID: 28944135      PMCID: PMC5608923          DOI: 10.5582/irdr.2017.01040

Source DB:  PubMed          Journal:  Intractable Rare Dis Res        ISSN: 2186-3644


  30 in total

1.  Targeted next-generation sequencing identification of a novel missense mutation of the SKIV2L gene in a patient with trichohepatoenteric syndrome.

Authors:  Bixia Zheng; Jian Pan; Yu Jin; Chunli Wang; Zhifeng Liu
Journal:  Mol Med Rep       Date:  2016-07-11       Impact factor: 2.952

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

Authors:  Alexandre Fabre; Nicolas André; Anne Breton; Pierre Broué; Catherine Badens; Bertrand Roquelaure
Journal:  Am J Med Genet A       Date:  2007-03-15       Impact factor: 2.802

3.  Novel mutations in SKIV2L and TTC37 genes in Malaysian children with trichohepatoenteric syndrome.

Authors:  Way Seah Lee; Kai Ming Teo; Ruey Terng Ng; Sze Yee Chong; Boon Pin Kee; Kek Heng Chua
Journal:  Gene       Date:  2016-04-12       Impact factor: 3.688

4.  Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome.

Authors:  D Oz-Levi; B Weiss; A Lahad; S Greenberger; B Pode-Shakked; R Somech; T Olender; P Tatarsky; D Marek-Yagel; E Pras; Y Anikster; D Lancet
Journal:  Clin Genet       Date:  2014-10-21       Impact factor: 4.438

5.  Expanding phenotypic and allelic heterogeneity of tricho-hepato-enteric syndrome.

Authors:  Dorota M Monies; Zuhair Rahbeeni; Mohamed Abouelhoda; Ewa A Naim; Banan Al-Younes; Brian F Meyer; Ali Al-Mehaidib
Journal:  J Pediatr Gastroenterol Nutr       Date:  2015-03       Impact factor: 2.839

6.  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

7.  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

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.  Trichohepatoenteric Syndrome or Syndromic Diarrhea-Report of Three Members in a Family, First Report from Iran.

Authors:  F E Mahjoub; F Imanzadeh; S Mahdavi Izadi; A Nahali Moghaddam
Journal:  Case Rep Pathol       Date:  2016-01-06
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  8 in total

1.  Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric Syndrome.

Authors:  Iddo Vardi; Ortal Barel; Michal Sperber; Michael Schvimer; Moran Nunberg; Michael Field; Jodie Ouahed; Dina Marek-Yagel; Lael Werner; Yael Haberman; Avishay Lahad; Yair Anikster; Gideon Rechavi; Iris Barshack; Joshua J McElwee; Joseph Maranville; Raz Somech; Scott B Snapper; Batia Weiss; Dror S Shouval
Journal:  Dig Dis Sci       Date:  2018-02-26       Impact factor: 3.199

Review 2.  Pathogenic insights from genetic causes of autoinflammatory inflammasomopathies and interferonopathies.

Authors:  Bin Lin; Raphaela Goldbach-Mansky
Journal:  J Allergy Clin Immunol       Date:  2021-12-08       Impact factor: 10.793

3.  Case Report: A Novel Homozygous Frameshift Mutation of the SKIV2L Gene in a Trichohepatoenteric Syndrome Patient Presenting With Short Stature, Premature Ovarian Failure, and Osteoporosis.

Authors:  Minyi Yang; Yu Jiang; Xinyu Shao
Journal:  Front Genet       Date:  2022-04-27       Impact factor: 4.772

4.  Novel TTC37 mutations in a patient with Trichohepatoenteric syndrome: a case report and literature review.

Authors:  Jinzhi Gao; Xiaolin Hu; Wei Hu; Xuan Sun; Ling Chen
Journal:  Transl Pediatr       Date:  2022-06

5.  Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management.

Authors:  Sarah K Baxter; Tom Walsh; Silvia Casadei; Mary M Eckert; Eric J Allenspach; David Hagin; Gesmar Segundo; Ming K Lee; Suleyman Gulsuner; Brian H Shirts; Kathleen E Sullivan; Michael D Keller; Troy R Torgerson; Mary-Claire King
Journal:  J Allergy Clin Immunol       Date:  2021-04-20       Impact factor: 10.793

6.  Trichohepatoenteric syndrome: A rare mutation in SKIV2L gene in the first Balkan reported case.

Authors:  Ioannis Xinias; Antigoni Mavroudi; Dimitrios Mouselimis; Anastasios Tsarouchas; Konstantina Vasilaki; Ioannis Roilides; Florence Lacaille; Olga Giouleme
Journal:  SAGE Open Med Case Rep       Date:  2018-10-30

7.  A Case of Mild Trichohepatoenteric Syndrome With New Variant Mutation in SKIV2L Gene: Case Report.

Authors:  Rawia F Albar; Mohammed S Alghamdi; Enad F Alsulimani; Ahmed M Almasrahi; Khalid A Alsalmi
Journal:  Cureus       Date:  2021-11-09

8.  Tricho-hepato-enteric syndrome: Retrospective multicenter experience in Saudi Arabia.

Authors:  Badr M Alsaleem; Mohammed Hasosah; Amna Basheer M Ahmed; Maher M Al Hatlani; Aziz Helal Alanazi; Abdulrahman Al-Hussaini; Ali T Asery; Khalid A Alghamdi; Muhanad M AlRuwaithi; Musa Ali M Khormi; Ahmed Al Sarkhy; Ali S Alshamrani
Journal:  Saudi J Gastroenterol       Date:  2022 Mar-Apr       Impact factor: 2.485

  8 in total

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