A Case of LEOPARD Syndrome / 대한피부과학회지
Korean Journal of Dermatology
;
: 949-952, 2005.
Article
Dans Coréen
| WPRIM
| ID: wpr-196337
ABSTRACT
LEOPARD syndrome is an autosomal dominantly inherited multiple congenital anomaly syndrome with high penetrance and a markedly variable expression. LEOPARD is an acronym of lentigines, electrocardiographic conduction defects, ocular hypertelorism, pulmonary stenosis, abnormalities of the genitalia, retardation of growth, and deafness. We report a typical case of LEOPARD syndrome which developed in an 11-year-old girl who had symptoms of lentigines, EKG abnormality, ocular hypertelorism, pulmonary stenosis, growth retardation, and sensorineural hearing loss.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Sténose de la valve pulmonaire
/
Pénétrance
/
Surdité
/
Syndrome LEOPARD
/
Panthera
/
Électrocardiographie
/
Système génital
/
Surdité neurosensorielle
/
Hypertélorisme
/
Lentigo
Limites du sujet:
Enfant
/
Femelle
/
Humains
langue:
Coréen
Texte intégral:
Korean Journal of Dermatology
Année:
2005
Type:
Article
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