Literature DB >> 15912410

Cerebellar and cerebral atrophy in trichothiodystrophy.

Hye-Kyung Yoon1, Michael A Sargent, Julie S Prendiville, Kenneth J Poskitt.   

Abstract

Trichothiodystrophy is a rare neuroectodermal disorder of autosomal recessive inheritance that is characterized by brittle hair, nail dysplasia, ichthyosis, mental retardation, and gonadal failure. We describe a female patient whose cranial MRI revealed almost total lack of myelination in the supratentorial white matter, which is similar to the previously described cases. In addition, there was progressive cerebellar and cerebral atrophy, which has not been well documented in association with trichothiodystrophy.

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Year:  2005        PMID: 15912410     DOI: 10.1007/s00247-005-1495-6

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  13 in total

1.  Tay's syndrome: MRI.

Authors:  L Porto; R Weis; C Schulz; P Reichel; H Lanfermann; F E Zanella
Journal:  Neuroradiology       Date:  2000-11       Impact factor: 2.804

2.  Trichothiodystrophy with severe cardiac and neurological involvement in two sisters.

Authors:  S P Toelle; E Valsangiacomo; E Boltshauser
Journal:  Eur J Pediatr       Date:  2001-12       Impact factor: 3.183

3.  MRI of a very rare hereditary ectodermal dysplasia: PIBI(D)S.

Authors:  A Peserico; P A Battistella; P Bertoli
Journal:  Neuroradiology       Date:  1992       Impact factor: 2.804

4.  MR of progressive neurodegenerative change in treated Menkes' kinky hair disease.

Authors:  D E Johnsen; L Coleman; L Poe
Journal:  Neuroradiology       Date:  1991       Impact factor: 2.804

5.  The trichothiodystrophy syndrome of Pollitt.

Authors:  S Chapman
Journal:  Pediatr Radiol       Date:  1988

6.  The central nervous system in Tay syndrome.

Authors:  J R Ostergaard; T Christensen
Journal:  Neuropediatrics       Date:  1996-12       Impact factor: 1.947

Review 7.  Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.

Authors:  P H Itin; A Sarasin; M R Pittelkow
Journal:  J Am Acad Dermatol       Date:  2001-06       Impact factor: 11.527

8.  Central nervous system dysmyelination in PIBI(D)S syndrome: a further case.

Authors:  P A Battistella; A Peserico
Journal:  Childs Nerv Syst       Date:  1996-02       Impact factor: 1.475

9.  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

Review 10.  Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literature.

Authors:  R Civitelli; W H McAlister; S L Teitelbaum; M P Whyte
Journal:  J Bone Miner Res       Date:  1989-12       Impact factor: 6.741

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  3 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

Review 2.  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

3.  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

  3 in total

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