Rud's Syndrome
Annals of Dermatology
;
: 206-210, 2000.
Artigo
em Inglês
| WPRIM
| ID: wpr-123795
ABSTRACT
Rud's syndrome (RS), basically composed of ichthyosis, mental deficiency and hypogonadism, is a rare hereditary disease. Some varying dermatologic, neurologic, endocrinologic, ophthalmologic and musculoskeletal abnormalities have coincided with RS. No case of RS has been documented from Asian countries except one from Japan. We describe a 16-year-old girl who presented with lamellar ichthyosis, mental retardation, hypogonadism, short stature, alopecia, sparse eyebrows, strabismus, cataracts, and congenital dislocation of the hip. To our knowledge, RS coexisting congenital dislocation of the hip herein is the first case in English literature.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Catarata
/
Estrabismo
/
Ictiose Lamelar
/
Povo Asiático
/
Luxações Articulares
/
Alopecia
/
Sobrancelhas
/
Doenças Genéticas Inatas
/
Quadril
/
Hipogonadismo
Limite:
Adolescente
/
Feminino
/
Humanos
País/Região como assunto:
Ásia
Idioma:
Inglês
Revista:
Annals of Dermatology
Ano de publicação:
2000
Tipo de documento:
Artigo
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