Rud's Syndrome
Annals of Dermatology
;
: 206-210, 2000.
Article
Dans Anglais
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Cataracte
/
Strabisme
/
Ichtyose lamellaire
/
Asiatiques
/
Luxations
/
Alopécie
/
Sourcils
/
Maladies génétiques congénitales
/
Hanche
/
Hypogonadisme
Limites du sujet:
Adolescent
/
Femelle
/
Humains
Pays comme sujet:
Asie
langue:
Anglais
Texte intégral:
Annals of Dermatology
Année:
2000
Type:
Article
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