Literature DB >> 11151695

Tay's syndrome: MRI.

L Porto1, R Weis, C Schulz, P Reichel, H Lanfermann, F E Zanella.   

Abstract

Tay's syndrome is a trichothiodystrophy associated with congenital ichthyosis. We report the findings on MRI and spectroscopy in a young girl with sparse, short, ruffled hair, dry skin and delayed milestones. T2-weighted images showed prominent diffuse confluent increase in signal symmetrically in all the supratentorial white matter. These findings are similar to those in a previously described case, and consistent with dysmyelination. Spectroscopy showed increased myoinositol and decreased choline.

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Year:  2000        PMID: 11151695     DOI: 10.1007/s002340000443

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  4 in total

1.  Ocular manifestations of trichothiodystrophy.

Authors:  Brian P Brooks; Amy H Thompson; Janine A Clayton; Chi-Chao Chan; Deborah Tamura; Wadih M Zein; Delphine Blain; Casey Hadsall; John Rowan; Kristen E Bowles; Sikandar G Khan; Takahiro Ueda; Jennifer Boyle; Kyu-Seon Oh; John J DiGiovanna; Kenneth H Kraemer
Journal:  Ophthalmology       Date:  2011-09-28       Impact factor: 12.079

2.  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 3.  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

4.  Trichothiodystrophy with dysmyelination and central osteosclerosis.

Authors:  J H Harreld; E C Smith; N S Prose; P K Puri; D P Barboriak
Journal:  AJNR Am J Neuroradiol       Date:  2010-01       Impact factor: 4.966

  4 in total

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