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A Case of Hypomelanosis of Ito with Hemimegalencephaly
Article en Ko | WPRIM | ID: wpr-154007
Biblioteca responsable: WPRO
ABSTRACT
Hypomelanosis of Ito is a congenital neurocutaneous syndrome with a particular pattern of streaks, patches and swirling hypopigmentation over variable portions of the body surface. Multiple extracutaneous abnormalities involving the central nervous system, musculoskeletal structures and the eyes occur in over two-thirds of the cases. This report describes a patient with typical unilateral cutaneous lesions associated with extracutaneous features, including hypertrophy of the cerebral hemisphere contralateral to the cutaneous hypopigmentation. Chromosomal analysis of fibroblasts of depigmented skin obtained from the patients showed mosaicism.
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Texto completo: 1 Base de datos: WPRIM Asunto principal: Piel / Sistema Nervioso Central / Hipopigmentación / Síndromes Neurocutáneos / Cerebro / Malformaciones del Desarrollo Cortical / Fibroblastos / Hipertrofia / Mosaicismo Límite: Humans Idioma: Ko Revista: Journal of the Korean Pediatric Society Año: 2000 Tipo del documento: Article
Texto completo: 1 Base de datos: WPRIM Asunto principal: Piel / Sistema Nervioso Central / Hipopigmentación / Síndromes Neurocutáneos / Cerebro / Malformaciones del Desarrollo Cortical / Fibroblastos / Hipertrofia / Mosaicismo Límite: Humans Idioma: Ko Revista: Journal of the Korean Pediatric Society Año: 2000 Tipo del documento: Article