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Trichohepatoenteric syndrome

MedGen UID:
347405
Concept ID:
C1857276
Disease or Syndrome
Synonyms: Syndromic diarrhea; THE SYNDROME; Tricho-hepato-enteric syndrome
SNOMED CT: Tricho-hepato-enteric syndrome (703406006); Trichohepatoenteric syndrome (703406006); Phenotypic diarrhea of infancy (703406006); Syndromic diarrhea (703406006); Fatal infantile diarrhea with trichorrhexis nodosa (703406006); Intractable diarrhea with phenotypic anomalies (703406006)
Modes of inheritance:
Autosomal recessive inheritance
MedGen UID:
141025
Concept ID:
C0441748
Intellectual Product
Source: Orphanet
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).
 
Monarch Initiative: MONDO:0009105
OMIM®: 222470
OMIM® Phenotypic series: PS222470
Orphanet: ORPHA84064

Definition

Although the spectrum of phenotypic expression in trichohepatoenteric syndrome (THES) is broad, the characteristic features include intrauterine growth retardation, woolly hair, facial dysmorphism, intractable diarrhea in infancy requiring total parenteral nutrition, and immunodepression. Hepatic involvement contributes to the poor prognosis of affected patients (summary by Fabre et al., 2007). Genetic Heterogeneity of Trichohepatoenteric Syndrome Trichohepatoenteric syndrome-2 (THES2; 614602) is caused by mutation in the SKIV2L gene (SKIC2; 600478) on chromosome 6p21. Reviews Bourgeois et al. (2018) analyzed a cohort of 96 patients with THES from 85 different families, drawing from published reports (37 patients) and their own recruitment (59 patients). Approximately two-thirds of the patients carried biallelic TTC37 mutations, and one-third had SKIVL2 mutations; in 8 (8.3%) of the patients, only 1 mutation could be identified. Intractable diarrhea was present in 100% of patients regardless of genotype, with hair abnormalities (woolly, brittle, easily removable) present in 90%. Facial dysmorphisms were observed in 84% of clinically described patients, comprising primarily large forehead, broad nasal root, and hypertelorism. Intrauterine growth retardation was frequent, seen in 70% of TTC37-mutated patients and 86% of SKIV2L-mutated patients; however, there was no significant difference in postnatal growth between the 2 groups. Liver disease was common, and more frequent in patients with mutation in SKIV2L (88%) than in TTC37 (51%); findings ranged from elevated liver enzymes and hepatomegaly to fibrosis and cirrhosis. Immunodeficiency was reported in about half of clinically explored patients, presenting as low immunoglobulin count or lack of antibody response to immunization. In addition, approximately 40% to 50% of patients exhibited dermatologic abnormalities, mostly cafe-au-lait spots located on the lower limbs. Overall, the authors noted that THES patients with mutation in either gene exhibit remarkably similar clinical signs, involving primarily the gastrointestinal tract, hair, and face, and are indistinguishable in clinical practice. However, a few differences emerged from analysis of the cohort, with SKIV2L-associated THES showing an earlier onset and/or greater severity, with more severe liver disease and significantly smaller height and weight at birth. [from OMIM]

Additional description

From MedlinePlus Genetics
Trichohepatoenteric syndrome is a condition that affects the hair (tricho-), liver (hepato-), and intestines (enteric), as well as other tissues and organs in the body. This condition is also known as syndromic diarrhea because chronic, difficult-to-treat diarrhea is one of its major features. Within the first few weeks of life, affected infants develop watery diarrhea that occurs multiple times per day. Even with nutritional support through intravenous feedings (parenteral nutrition), many of these children experience failure to thrive, which means they do not gain weight or grow at the expected rate. Most children with trichohepatoenteric syndrome are small at birth, and they remain shorter than their peers throughout life.

Abnormal hair is another feature of trichohepatoenteric syndrome. Hair in affected individuals is described as wooly, brittle, patchy, and easily pulled out. Under a microscope, some strands of hair can be seen to vary in diameter, with thicker and thinner spots. This feature is known as trichorrhexis nodosa.

Other signs and symptoms of trichohepatoenteric syndrome can include liver disease; skin abnormalities; and distinctive facial features, including a wide forehead, a broad base of the nose, and widely spaced eyes. Overall, the facial features are described as "coarse." Most affected individuals also experience immune system abnormalities that can make them prone to developing infections. Less commonly, trichohepatoenteric syndrome is associated with heart (cardiac) abnormalities. Mild intellectual disability has been reported in at least half of all children with the condition.

Trichohepatoenteric syndrome is often life-threatening in childhood, particularly in children who develop liver disease or severe infections.  https://medlineplus.gov/genetics/condition/trichohepatoenteric-syndrome

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVTrichohepatoenteric syndrome

Recent clinical studies

Etiology

Wang J, Fiori PL, Capobianco G, Carru C, Chen Z
Front Endocrinol (Lausanne) 2024;15:1275419. Epub 2024 Jan 22 doi: 10.3389/fendo.2024.1275419. PMID: 38318294Free PMC Article
Alsaleem BM, Hasosah M, Ahmed ABM, Al Hatlani MM, Alanazi AH, Al-Hussaini A, Asery AT, Alghamdi KA, AlRuwaithi MM, Khormi MAM, Al Sarkhy A, Alshamrani AS
Saudi J Gastroenterol 2022 Mar-Apr;28(2):135-142. doi: 10.4103/sjg.sjg_200_21. PMID: 34414925Free PMC Article
Vély F, Barlogis V, Marinier E, Coste ME, Dubern B, Dugelay E, Lemale J, Martinez-Vinson C, Peretti N, Perry A, Bourgeois P, Badens C, Goulet O, Hugot JP, Farnarier C, Fabre A
Front Immunol 2018;9:1036. Epub 2018 May 11 doi: 10.3389/fimmu.2018.01036. PMID: 29868001Free PMC Article
Monies DM, Rahbeeni Z, Abouelhoda M, Naim EA, Al-Younes B, Meyer BF, Al-Mehaidib A
J Pediatr Gastroenterol Nutr 2015 Mar;60(3):352-6. doi: 10.1097/MPG.0000000000000627. PMID: 25714577
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
Arch Dis Child 2014 Jan;99(1):35-8. Epub 2013 Oct 9 doi: 10.1136/archdischild-2013-304016. PMID: 24108068

Diagnosis

Wang J, Fiori PL, Capobianco G, Carru C, Chen Z
Front Endocrinol (Lausanne) 2024;15:1275419. Epub 2024 Jan 22 doi: 10.3389/fendo.2024.1275419. PMID: 38318294Free PMC Article
Lee KY, Bremner R, Hartley J, Protheroe S, Haller W, Johnson T, Whyte L
Am J Med Genet A 2024 Feb;194(2):141-149. Epub 2023 Sep 27 doi: 10.1002/ajmg.a.63409. PMID: 37753667
Dorum S, Gorukmez O
Am J Med Genet A 2021 Oct;185(10):2873-2877. Epub 2021 May 26 doi: 10.1002/ajmg.a.62354. PMID: 34037310
Poulton C, Pathak G, Mina K, Lassman T, Azmanov DN, McCormack E, Broley S, Dreyer L, Gration D, Taylor E, OSullivan M, Siafarikis A, Ravikumara M, Dawkins H, Pachter N, Baynam G
Gene 2019 May 30;699:110-114. Epub 2019 Mar 4 doi: 10.1016/j.gene.2019.02.059. PMID: 30844479Free PMC Article
Vély F, Barlogis V, Marinier E, Coste ME, Dubern B, Dugelay E, Lemale J, Martinez-Vinson C, Peretti N, Perry A, Bourgeois P, Badens C, Goulet O, Hugot JP, Farnarier C, Fabre A
Front Immunol 2018;9:1036. Epub 2018 May 11 doi: 10.3389/fimmu.2018.01036. PMID: 29868001Free PMC Article

Therapy

Wang J, Fiori PL, Capobianco G, Carru C, Chen Z
Front Endocrinol (Lausanne) 2024;15:1275419. Epub 2024 Jan 22 doi: 10.3389/fendo.2024.1275419. PMID: 38318294Free PMC Article
Rambhia PH, Hanna R, Bergfeld WF
Int J Dermatol 2018 Jan;57(1):89-91. Epub 2017 Nov 11 doi: 10.1111/ijd.13820. PMID: 29130476
Hiejima E, Yasumi T, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Okafuji I, Yorifuji T, Tanaka T, Izawa K, Kawai T, Nishikomori R, Heike T
Medicine (Baltimore) 2017 Nov;96(46):e8601. doi: 10.1097/MD.0000000000008601. PMID: 29145277Free PMC Article
Busoni VB, Lemale J, Dubern B, Frangi F, Bourgeois P, Orsi M, Badens C, Fabre A
J Pediatr Gastroenterol Nutr 2017 Jan;64(1):37-41. doi: 10.1097/MPG.0000000000001218. PMID: 28027214

Prognosis

Duclaux-Loras R, Lebreton C, Berthelet J, Charbit-Henrion F, Nicolle O, Revenu des Courtils C, Waich S, Valovka T, Khiat A, Rabant M, Racine C, Guerrera IC, Baptista J, Mahe MM, Hess MW, Durel B, Lefort N, Banal C, Parisot M, Talbotec C, Lacaille F, Ecochard-Dugelay E, Demir AM, Vogel GF, Faivre L, Rodrigues A, Fowler D, Janecke AR, Müller T, Huber LA, Rodrigues-Lima F, Ruemmele FM, Uhlig HH, Del Bene F, Michaux G, Cerf-Bensussan N, Parlato M
J Clin Invest 2022 May 16;132(10) doi: 10.1172/JCI154997. PMID: 35575086Free PMC Article
Alsaleem BM, Hasosah M, Ahmed ABM, Al Hatlani MM, Alanazi AH, Al-Hussaini A, Asery AT, Alghamdi KA, AlRuwaithi MM, Khormi MAM, Al Sarkhy A, Alshamrani AS
Saudi J Gastroenterol 2022 Mar-Apr;28(2):135-142. doi: 10.4103/sjg.sjg_200_21. PMID: 34414925Free PMC Article
Dorum S, Gorukmez O
Am J Med Genet A 2021 Oct;185(10):2873-2877. Epub 2021 May 26 doi: 10.1002/ajmg.a.62354. PMID: 34037310
Vardi I, Barel O, Sperber M, Schvimer M, Nunberg M, Field M, Ouahed J, Marek-Yagel D, Werner L, Haberman Y, Lahad A, Anikster Y, Rechavi G, Barshack I, McElwee JJ, Maranville J, Somech R, Snapper SB, Weiss B, Shouval DS
Dig Dis Sci 2018 May;63(5):1192-1199. Epub 2018 Feb 26 doi: 10.1007/s10620-018-4983-x. PMID: 29484573Free PMC Article
Lee WS, Teo KM, Ng RT, Chong SY, Kee BP, Chua KH
Gene 2016 Jul 15;586(1):1-6. Epub 2016 Apr 12 doi: 10.1016/j.gene.2016.03.049. PMID: 27050310

Clinical prediction guides

Ozturk M, Ates K, Esener Z, Mutlu H, Aydogmus C, Boztug K, Sarac H, Gezdirici A, Dogan M, Beser OF, Varol FI, Gokce IK, Ozdemir R, Tekedereli I
Mol Biol Rep 2024 Jun 14;51(1):736. doi: 10.1007/s11033-024-09656-6. PMID: 38874671
Laffleur B, Batista CR, Zhang W, Lim J, Yang B, Rossille D, Wu L, Estrella J, Rothschild G, Pefanis E, Basu U
Sci Immunol 2022 Jun 3;7(72):eabn2738. doi: 10.1126/sciimmunol.abn2738. PMID: 35658015Free PMC Article
Duclaux-Loras R, Lebreton C, Berthelet J, Charbit-Henrion F, Nicolle O, Revenu des Courtils C, Waich S, Valovka T, Khiat A, Rabant M, Racine C, Guerrera IC, Baptista J, Mahe MM, Hess MW, Durel B, Lefort N, Banal C, Parisot M, Talbotec C, Lacaille F, Ecochard-Dugelay E, Demir AM, Vogel GF, Faivre L, Rodrigues A, Fowler D, Janecke AR, Müller T, Huber LA, Rodrigues-Lima F, Ruemmele FM, Uhlig HH, Del Bene F, Michaux G, Cerf-Bensussan N, Parlato M
J Clin Invest 2022 May 16;132(10) doi: 10.1172/JCI154997. PMID: 35575086Free PMC Article
Vardi I, Barel O, Sperber M, Schvimer M, Nunberg M, Field M, Ouahed J, Marek-Yagel D, Werner L, Haberman Y, Lahad A, Anikster Y, Rechavi G, Barshack I, McElwee JJ, Maranville J, Somech R, Snapper SB, Weiss B, Shouval DS
Dig Dis Sci 2018 May;63(5):1192-1199. Epub 2018 Feb 26 doi: 10.1007/s10620-018-4983-x. PMID: 29484573Free PMC Article
Michaux G, Massey-Harroche D, Nicolle O, Rabant M, Brousse N, Goulet O, Le Bivic A, Ruemmele FM
Biol Cell 2016 Jan;108(1):19-28. Epub 2015 Dec 8 doi: 10.1111/boc.201500034. PMID: 26526116

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