A Case of LEOPARD Syndrome / 대한피부과학회지
Korean Journal of Dermatology
;
: 949-952, 2005.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pulmonary Valve Stenosis
/
Penetrance
/
Deafness
/
LEOPARD Syndrome
/
Panthera
/
Electrocardiography
/
Genitalia
/
Hearing Loss, Sensorineural
/
Hypertelorism
/
Lentigo
Limits:
Child
/
Female
/
Humans
Language:
Korean
Journal:
Korean Journal of Dermatology
Year:
2005
Type:
Article
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