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Aplasia Cutis Congenita in Two Siblings / 대한피부과학회지
Korean Journal of Dermatology ; : 714-717, 2012.
Artigo em Coreano | WPRIM | ID: wpr-41989
ABSTRACT
Aplasia cutis congenita is a rare congenital condition, characterized by localized absence of epidermis, dermis, and in some cases, subcutaneous tissues. About 80% of the patients with aplasia cutis congenita have involvement of the scalp. Aplasia cutis congenita, not involving the scalp, appears to be linear lesions with a symmetrical pattern of distribution on the trunk and limbs. Most reported cases are sporadic, but a few cases have been reported to have familial occurrence. There is no unifying theory for the pathogenesis and etiology. Herein, we report a 1-day-old female infant and her 4-year-old sister with unilateral aplasia cutis congenita on their legs. No similar conditions and other associated congenital anomalies were found in their family. There was no sign of teratogenic causes, such as intrauterine infections, drugs or chemical agents.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Couro Cabeludo / Displasia Ectodérmica / Pré-Escolar / Derme / Tela Subcutânea / Irmãos / Epiderme / Extremidades / Perna (Membro) Limite: Feminino / Humanos / Lactente Idioma: Coreano Revista: Korean Journal of Dermatology Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Couro Cabeludo / Displasia Ectodérmica / Pré-Escolar / Derme / Tela Subcutânea / Irmãos / Epiderme / Extremidades / Perna (Membro) Limite: Feminino / Humanos / Lactente Idioma: Coreano Revista: Korean Journal of Dermatology Ano de publicação: 2012 Tipo de documento: Artigo