A case of LEOPARD syndrome with cor triatriatum / 대한내과학회지
Korean Journal of Medicine
;
: 99-103, 2003.
Artigo
em Coreano
| WPRIM
| ID: wpr-211188
ABSTRACT
The LEOPARD syndrome is an acronym and serves as a mnemonic for the features of this autosomal dominant syndrome L - lentigines (multiple), E - electrocardiographic conduction abnormalities, O - ocular hypertelorism, P - pulmonary stenosis, A - abnormalities of genitalia, R - retardation of growth, and D - deafness (sensoryneural). The main features of the syndrome are multiple lentigines in combination with congenital heart malformations. These frequently accompanied cardiac abnormalities are pulmonary stenosis, hypertrophic cardiomyopathy, and various ECG abnormalities. It is advisable to make cardiac evaluation in a patient with LEOPARD syndrome in spite of no clinical symptoms or signs, since cardiac dysfunction may be progressive or developed later. We experienced a case of this syndrome in a 31 year-old female, presenting multiple lentigines, ocular hypertelorism, and congenital cardiac abnormalities of incomplete right bundle branch block and cor triatriatum. We report the case with brief literature review.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Estenose da Valva Pulmonar
/
Cardiomiopatia Hipertrófica
/
Coração Triatriado
/
Bloqueio de Ramo
/
Surdez
/
Síndrome LEOPARD
/
Panthera
/
Eletrocardiografia
/
Genitália
/
Coração
Limite:
Adulto
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Medicine
Ano de publicação:
2003
Tipo de documento:
Artigo
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