A Case of Wilson's Disease in Patient with Mildly Elevated Liver Enzymes / 가정의학회지
Korean Journal of Family Medicine
;
: 205-208, 2011.
Artigo
em Inglês
| WPRIM
| ID: wpr-35455
ABSTRACT
Wilson's disease is an autosomal recessive disorder affecting copper transport; it results in the accumulation of copper in the liver, brain, and other organs. Wilson's disease is the most common inherited liver disease with more than 500 cases reported in Korea. An impairment in biliary excretion process leads to copper accumulation in the liver, which progressively damages the liver, leading to cirrhosis. Since effective treatment is available for this disease, early and correct diagnosis is very important. Here, we report a case of Wilson's disease with mildly elevated liver enzyme levels in a 29-year-old breast-feeding woman with weight loss.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Fibrose
/
Encéfalo
/
Redução de Peso
/
Cobre
/
Hepatite
/
Degeneração Hepatolenticular
/
Coreia (Geográfico)
/
Fígado
/
Hepatopatias
Limite:
Adulto
/
Feminino
/
Humanos
País/Região como assunto:
Ásia
Idioma:
Inglês
Revista:
Korean Journal of Family Medicine
Ano de publicação:
2011
Tipo de documento:
Artigo
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