The Challenges of Diagnosing and Following Wilson Disease in the Presence of Proteinuria / 대한소아소화기영양학회지
Pediatric Gastroenterology, Hepatology & Nutrition
;
: 139-142, 2016.
Artículo
en Inglés
| WPRIM
| ID: wpr-148721
ABSTRACT
The coexistence of Wilson disease with Alport syndrome has not previously been reported. The diagnosis of Wilson disease and its ongoing monitoring is challenging when associated with an underlying renal disease such as Alport syndrome. Proteinuria can lead to low ceruloplasmin since it is among serum proteins inappropriately filtered by the damaged glomerulus, and can also lead to increased urinary loss of heavy metals such as zinc and copper. Elevated transaminases may be attributed to dyslipidemia or drug induced hepatotoxicity. The accurate diagnosis of Wilson disease is essential for targeted therapy and improved prognosis. We describe a patient with a diagnosis of Alport syndrome who has had chronic elevation of transaminases eventually diagnosed with Wilson disease based on liver histology and genetics.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Pronóstico
/
Proteinuria
/
Zinc
/
Ceruloplasmina
/
Proteínas Sanguíneas
/
Metales Pesados
/
Cobre
/
Diagnóstico
/
Dislipidemias
/
Genética
Tipo de estudio:
Estudio diagnóstico
/
Estudio pronóstico
Límite:
Humanos
Idioma:
Inglés
Revista:
Pediatric Gastroenterology, Hepatology & Nutrition
Año:
2016
Tipo del documento:
Artículo
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