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Artigo em Coreano | WPRIM | ID: wpr-188136

RESUMO

Leopard syndrome, a feature of a syndrome, is a acronym of Lentiginosis, Electrocardiographic conduction abnormalities, Ocular hypertelorism, Pulmonic stenosis, Abnormal genitalia, Retardation of growth, and Deafness. It is one of the autosomal dominant neurocutaneous traits accompanied by neurologic abnormality. We have experienced a case of Leopoard syndrome associated with 46,XX pure gonadal dysgenesis, which was diagnosed by laparoscopic biopsy, karyotyping, and dermatologic consultation. So we report this case with a brief review of literatures. In our knowledge, this very rare case is presented for the first time in Korea.


Assuntos
Biópsia , Surdez , Eletrocardiografia , Genitália , Disgenesia Gonadal , Gônadas , Hipertelorismo , Cariotipagem , Coreia (Geográfico) , Lentigo , Síndrome LEOPARD , Panthera , Estenose da Valva Pulmonar
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