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Tay syndrome.
Indian J Pediatr ; 2008 Mar; 75(3): 288-90
Article Dans Anglais | IMSEAR | ID: sea-80036
ABSTRACT
Tay syndrome or IBIDS is a rare autosomal recessive genetic disorder characterized by congenital ichthyosis and abnormal brittle hair (trichothiodystrophy). Other features include photosensitivity, abnormal nails and multiple developmental defects affecting organs mainly derived from neuroectoderm. The exact prevalence of this condition is not known, but up to 1991, clinical data of 15 cases with IBIDS were published .We report a case of Tay syndrome with additional features of Duane's retraction syndrome and Perthes disease, which have not yet been reported in literature.
Sujets)
Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) Sujet Principal: Humains / Mâle / Enfant / Érythrodermie ichtyosiforme congénitale / Consanguinité / Diagnostic différentiel / Poils Type d'étude: Etude diagnostique langue: Anglais Texte intégral: Indian J Pediatr Année: 2008 Type: Article

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Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) Sujet Principal: Humains / Mâle / Enfant / Érythrodermie ichtyosiforme congénitale / Consanguinité / Diagnostic différentiel / Poils Type d'étude: Etude diagnostique langue: Anglais Texte intégral: Indian J Pediatr Année: 2008 Type: Article