| Literature DB >> 17504703 |
R Jiménez-Puya1, J C Moreno-Giménez, F Camacho-Martínez, J Ferrando-Barbera, R Grimalt.
Abstract
Trichothiodystrophy comprises a heterogeneous group of autosomal recessive entities. This fact gives rise to different interrelated neuroectodermal disorders. From a structural point of view these features are the result of the low tissue sulfur content. We report a case of trichothiodystrophy initially classified as Tay syndrome that based on clinical features, complementary exams as well as on the disease evolution was labelled as PIBIDS syndrome.Entities:
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Year: 2007 PMID: 17504703
Source DB: PubMed Journal: Actas Dermosifiliogr ISSN: 0001-7310