Literature DB >> 11795681

Trichothiodystrophy with severe cardiac and neurological involvement in two sisters.

S P Toelle1, E Valsangiacomo, E Boltshauser.   

Abstract

UNLABELLED: Trichothiodystrophy or sulphur-deficient brittle hair is a clinical marker for several autosomal recessive neurocutaneous syndromes. The typical hair abnormality is frequently associated with many alterations affecting the skin, nervous system, eyes and bones as well as the immune, gonadal and endocrine systems. We report the first cases of dilated cardiomyopathy in two sisters with trichothiodystrophy, leading to cerebral infarction in the younger one. In addition, both suffer from severe hearing impairment, osteosclerosis, and psychomotor retardation with central hypomyelination.
CONCLUSION: Severe cardiac involvement and stroke may be associated features of trichothiodystrophy.

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Year:  2001        PMID: 11795681     DOI: 10.1007/s004310100845

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  8 in total

1.  Cerebellar and cerebral atrophy in trichothiodystrophy.

Authors:  Hye-Kyung Yoon; Michael A Sargent; Julie S Prendiville; Kenneth J Poskitt
Journal:  Pediatr Radiol       Date:  2005-05-24

Review 2.  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

Review 3.  DNA damage in the oligodendrocyte lineage and its role in brain aging.

Authors:  Kai-Hei Tse; Karl Herrup
Journal:  Mech Ageing Dev       Date:  2016-05-26       Impact factor: 5.432

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.  Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degeneration.

Authors:  Mariam B Totonchy; Deborah Tamura; Matthew S Pantell; Christopher Zalewski; Porcia T Bradford; Saumil N Merchant; Joseph Nadol; Sikandar G Khan; Raphael Schiffmann; Tyler Mark Pierson; Edythe Wiggs; Andrew J Griffith; John J DiGiovanna; Kenneth H Kraemer; Carmen C Brewer
Journal:  Brain       Date:  2013-01       Impact factor: 13.501

6.  Bone fragility and decline in stem cells in prematurely aging DNA repair deficient trichothiodystrophy mice.

Authors:  Karin E M Diderich; Claudia Nicolaije; Matthias Priemel; Jan H Waarsing; Judd S Day; Renata M C Brandt; Arndt F Schilling; Sander M Botter; Harrie Weinans; Gijsbertus T J van der Horst; Jan H J Hoeijmakers; Johannes P T M van Leeuwen
Journal:  Age (Dordr)       Date:  2011-08-04

7.  Reduced levels of prostaglandin I2 synthase: a distinctive feature of the cancer-free trichothiodystrophy.

Authors:  Anita Lombardi; Lavinia Arseni; Roberta Carriero; Emmanuel Compe; Elena Botta; Debora Ferri; Martina Uggè; Giuseppe Biamonti; Fiorenzo A Peverali; Silvia Bione; Donata Orioli
Journal:  Proc Natl Acad Sci U S A       Date:  2021-06-29       Impact factor: 11.205

8.  Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP.

Authors:  Khadim Shah; Raja Hussain Ali; Muhammad Ansar; Kwanghyuk Lee; Muhammad Salman Chishti; Izoduwa Abbe; Biao Li; Joshua D Smith; Deborah A Nickerson; Jay Shendure; Paul J Coucke; Wouter Steyaert; Michael J Bamshad; Regie Lyn P Santos-Cortez; Suzanne M Leal; Wasim Ahmad
Journal:  BMC Med Genet       Date:  2016-02-16       Impact factor: 2.103

  8 in total

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