[Trichothiodystrophy: PIBIDS syndrome]. / Tricotiodistrofia: síndrome PIBIDS.
Actas Dermosifiliogr
; 98(3): 183-7, 2007 Apr.
Article
en Es
| MEDLINE
| ID: mdl-17504703
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.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Azufre
/
Síndromes Neurocutáneos
/
Enfermedades del Cabello
Límite:
Female
/
Humans
/
Infant
Idioma:
Es
Revista:
Actas Dermosifiliogr
Año:
2007
Tipo del documento:
Article