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Indian Pediatr ; 2010 Nov; 47(11): 977-978
Artigo em Inglês | IMSEAR | ID: sea-168708

RESUMO

Acute intermittent porphyria is a hereditary disorder characterized by deficient activity of the enzyme porphobilinogen deaminase. It manifests with occasional neurovisceral crises due to overproduction of porphyrin precursors. We report a 12 year old male child with acute intermittent porphyria, who presented with encephalopathy and transient blindness of cerebral origin.

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