Literature DB >> 10482949

Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis.

E Laiho1, K M Niemi, J Ignatius, J Kere, A Palotie, U Saarialho-Kere.   

Abstract

Autosomal recessive congenital ichthyosis (ARCI) is a group of inherited disorders of cornification in which progress has recently been made in the identification of pathogenic mechanisms causing the disease. Transglutaminase 1 (TGM1) has been found as a defective gene in a large fraction of patients with lamellar ichthyosis (LI), a severe inherited scaling disorder of the skin. We have previously performed molecular genetic studies of 38Finnish ARCI families and found six different mutations in 13 families of 38 (34%). In this study we compared the molecular genetic alterations with clinical and electron microscopic findings of these patients. Families were classified by electron microscopy in ichthyosis congenita (IC) types I, II, III, IV and a non-defined group. TGM 1 gene mutation was found in all of the IC type II and 1/3 of the IC type 1 families. Although electron microscopy is not always used to classify ARCI patients, it can distinguish groups which are parallel with molecular genetic findings. This finding might be useful in the classification of ARCI patients for further linkage studies. Clinically typical phenotype of the TGM1 mutation carrier includes large, thick, brownish scales, but ichthyosis of some of these patients tends to be milder.

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Year:  1999        PMID: 10482949     DOI: 10.1038/sj.ejhg.5200353

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  11 in total

Review 1.  Transglutaminase-1 gene mutations in autosomal recessive congenital ichthyosis: summary of mutations (including 23 novel) and modeling of TGase-1.

Authors:  Matthew L Herman; Sharifeh Farasat; Peter J Steinbach; Ming-Hui Wei; Ousmane Toure; Philip Fleckman; Patrick Blake; Sherri J Bale; Jorge R Toro
Journal:  Hum Mutat       Date:  2009-04       Impact factor: 4.878

2.  Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1.

Authors:  Nobuo Kuramoto; Toshihiro Takizawa; Takami Takizawa; Masato Matsuki; Hiroyuki Morioka; John M Robinson; Kiyofumi Yamanishi
Journal:  J Clin Invest       Date:  2002-01       Impact factor: 14.808

3.  Topical enzyme-replacement therapy restores transglutaminase 1 activity and corrects architecture of transglutaminase-1-deficient skin grafts.

Authors:  Karin Aufenvenne; Fernando Larcher; Ingrid Hausser; Blanca Duarte; Vinzenz Oji; Heike Nikolenko; Marcela Del Rio; Margitta Dathe; Heiko Traupe
Journal:  Am J Hum Genet       Date:  2013-09-19       Impact factor: 11.025

4.  A three-dimensional model of the human transglutaminase 1: insights into the understanding of lamellar ichthyosis.

Authors:  Karen M Boeshans; Timothy C Mueser; Bijan Ahvazi
Journal:  J Mol Model       Date:  2006-09-23       Impact factor: 1.810

5.  Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity.

Authors:  A Krebsová; W Küster; G G Lestringant; B Schulze; B Hinz; P M Frossard; A Reis; H C Hennies
Journal:  Am J Hum Genet       Date:  2001-06-07       Impact factor: 11.025

6.  Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA.

Authors:  S Farasat; M-H Wei; M Herman; D J Liewehr; S M Steinberg; S J Bale; P Fleckman; J R Toro
Journal:  J Med Genet       Date:  2008-10-23       Impact factor: 6.318

7.  Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.

Authors:  J Dahlqvist; J Klar; I Hausser; I Anton-Lamprecht; M Hellström Pigg; T Gedde-Dahl; A Gånemo; A Vahlquist; N Dahl
Journal:  J Med Genet       Date:  2007-06-08       Impact factor: 6.318

8.  Transglutaminase1 preferred substrate peptide K5 is an efficient tool in diagnosis of lamellar ichthyosis.

Authors:  Masashi Akiyama; Kaori Sakai; Teruki Yanagi; Satoshi Fukushima; Hironobu Ihn; Kiyotaka Hitomi; Hiroshi Shimizu
Journal:  Am J Pathol       Date:  2010-02-18       Impact factor: 4.307

9.  PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans.

Authors:  Anaïs Grall; Eric Guaguère; Sandrine Planchais; Susanne Grond; Emmanuelle Bourrat; Ingrid Hausser; Christophe Hitte; Matthieu Le Gallo; Céline Derbois; Gwang-Jin Kim; Laëtitia Lagoutte; Frédérique Degorce-Rubiales; Franz P W Radner; Anne Thomas; Sébastien Küry; Emmanuel Bensignor; Jacques Fontaine; Didier Pin; Robert Zimmermann; Rudolf Zechner; Mark Lathrop; Francis Galibert; Catherine André; Judith Fischer
Journal:  Nat Genet       Date:  2012-01-15       Impact factor: 38.330

10.  Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis.

Authors:  A Terrinoni; V Serra; A Codispoti; E Talamonti; L Bui; R Palombo; M Sette; E Campione; B Didona; M Annicchiarico-Petruzzelli; G Zambruno; G Melino; E Candi
Journal:  Cell Death Dis       Date:  2012-10-25       Impact factor: 8.469

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