Four Generations of Piebaldism / 대한피부과학회지
Korean Journal of Dermatology
;
: 1273-1276, 2002.
Artigo
em Coreano
| WPRIM
| ID: wpr-28379
ABSTRACT
Piebaldism is an uncommon autosomal dominant genetic disorder. It is characterized by amelanotic macules or patches, usually containing some hyperpigmented or normopigmented macules, of the central portion of the forehead, the chin, and the ventral aspect of the trunk and the limbs. A 10 year-old female patient had depigmented lesions on the abdomen and both legs, discovered one month after her birth. On the history taking, she had family history of four generations. We report a case of piebaldism showing typical autosomal dominant pattern.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Características da Família
/
Piebaldismo
/
Queixo
/
Parto
/
Abdome
/
Extremidades
/
Testa
/
Perna (Membro)
Limite:
Criança
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
2002
Tipo de documento:
Artigo
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