| Literature DB >> 20075106 |
J H Harreld1, E C Smith, N S Prose, P K Puri, D P Barboriak.
Abstract
Trichothiodystrophy (TTD) is a rare group of autosomal recessive disorders of DNA repair unified by the presence of sulfur-deficient brittle hair. We report a 3-year-old boy with classic clinical features of TTD, including ichthyosis, alopecia, developmental delay, and tiger-tail banding of the hair shaft on polarizing microscopy. Brain MR imaging showed both diffuse dysmyelination and osteosclerosis, findings that, in combination, may be specific for TTD.Entities:
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Year: 2010 PMID: 20075106 PMCID: PMC7964056 DOI: 10.3174/ajnr.A1665
Source DB: PubMed Journal: AJNR Am J Neuroradiol ISSN: 0195-6108 Impact factor: 4.966