Recurrent limb weakness as initial presentation of Wilson's disease.
Artículo
en Inglés
| IMSEAR
| ID: sea-64305
ABSTRACT
A 28-year-old normotensive euthyroid man presented with recurrent lower motor neuron type of weakness without sensory or autonomic involvement, with preserved reflexes. Systemic examination was significant for mild hepatosplenomegaly. Investigations revealed persistent hypokalemic, hyperchloremic, normal-anion-gap metabolic acidosis with deranged liver functions. Urine pH was 6.0 even after oral ammonium-chloride loading test. Type I renal tubular acidosis was diagnosed. A search for the etiology revealed bilateral Kayser-Fleischer ring, with low serum ceruloplasmin levels and high urinary copper, confirming it to be Wilson's disease.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Humanos
/
Masculino
/
Debilidad Muscular
/
Adulto
/
Diagnóstico Diferencial
/
Extremidades
/
Degeneración Hepatolenticular
Tipo de estudio:
Estudio diagnóstico
Idioma:
Inglés
Año:
2007
Tipo del documento:
Artículo
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