A case of hereditary hemorrhagic telangiectasia / 소아과
Korean Journal of Pediatrics
;
: 1018-1023, 2007.
Article
in English
| WPRIM
| ID: wpr-128437
ABSTRACT
Hereditary hemorrhagic telagiectasia (HHT), which is characterized by the classic triad of mucocutaneous telangiectases, arteriovenous malformations (AVMs) and inheritance, is an autosomal dominant disorder. The characteristic manifestations of HHT are all due to abnormalities of the vascular structure. This report deals with the case of a 14-year-old girl with typical features of HHT that include recurrent epistaxis, mucocutanous telangiectases, pulmonary and cerebral AVMs and a familial occurrence.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Arteriovenous Malformations
/
Recurrence
/
Telangiectasia, Hereditary Hemorrhagic
/
Telangiectasis
/
Wills
/
Epistaxis
/
Inheritance Patterns
Limits:
Adolescent
/
Female
/
Humans
Language:
English
Journal:
Korean Journal of Pediatrics
Year:
2007
Type:
Article
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