Literature DB >> 8205320

Syndromes associated with trichothiodystrophy.

J L Tolmie1, D de Berker, R Dawber, C Galloway, D W Gregory, A R Lehmann, J McClure, R J Pollitt, J B Stephenson.   

Abstract

Sparse, brittle, sulphur-deficient hair is an excellent marker for several autosomal recessive neurocutaneous syndromes. The term 'trichothiodystrophy' is commonly used in publications on such syndromes and the best characterized trichothiodystrophy syndrome is associated with skin photosensitivity and intellectual impairment. Patients with these three cardinal signs usually have an underlying DNA repair defect. Here we describe clinical and laboratory findings in two patients with trichothiodystrophy and defective DNA repair alongside findings in three other cases who have different trichothiodystrophy syndromes without defective DNA repair. These patients' features are discussed in the light of a practical classification scheme which is based upon a check-list of clinical abnormalities associated with trichothiodystrophy syndromes (Van Neste, 1991).

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Year:  1994        PMID: 8205320

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  6 in total

Review 1.  Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations.

Authors:  S Faghri; D Tamura; K H Kraemer; J J Digiovanna
Journal:  J Med Genet       Date:  2008-06-25       Impact factor: 6.318

2.  Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals.

Authors:  C Ahrens; M Grewe; M Berneburg; S Grether-Beck; X Quilliet; M Mezzina; A Sarasin; A R Lehmann; C F Arlett; J Krutmann
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-24       Impact factor: 11.205

3.  Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta.

Authors:  Roxana Moslehi; Anil Kumar; James L Mills; Xavier Ambroggio; Caroline Signore; Amiran Dzutsev
Journal:  Eur J Hum Genet       Date:  2012-01-11       Impact factor: 4.246

4.  Central osteosclerosis with trichothiodystrophy.

Authors:  Emma L Wakeling; Michele Cruwys; Mohnish Suri; Angela F Brady; Sarah E Aylett; Christine Hall
Journal:  Pediatr Radiol       Date:  2004-05-18

5.  Novel ERCC2 variant in trichothiodystrophy infant: the first case report in China.

Authors:  Jian-Dong Chen; Wei-Dong Liao; Ling-Ying Wen; Rong-Hua Zhong
Journal:  BMC Pediatr       Date:  2021-03-12       Impact factor: 2.125

6.  Ercc2/Xpd deficiency results in failure of digestive organ growth in zebrafish with elevated nucleolar stress.

Authors:  Jinmin Ma; Xuelian Shao; Fang Geng; Shuzhang Liang; Chunxiao Yu; Ruilin Zhang
Journal:  iScience       Date:  2022-08-17
  6 in total

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