Persistent transaminase elevation due to heterozygous (familial) apolipoprotein B deficiency.
Artículo
en Inglés
| IMSEAR
| ID: sea-64276
ABSTRACT
Homozygous apolipoprotein B deficiency can present with fatty liver and raised levels of transaminases. Subjects with heterozygous deficiency are almost always asymptomatic. We report an asymptomatic 26-year-old man with persistently raised transaminases, in whom the diagnosis of heterozygous (familial) apolipoprotein B deficiency was made on the basis of characteristic lipid profile.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Apolipoproteínas B
/
Humanos
/
Masculino
/
Aberraciones Cromosómicas
/
Adulto
/
Trastornos de los Cromosomas
/
Genes Dominantes
/
Transaminasas
/
Heterocigoto
/
Hipobetalipoproteinemias
Idioma:
Inglés
Año:
1997
Tipo del documento:
Artículo
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