Acute Intermittent Porphyria with Transient Cortical Blindness.
Indian Pediatr
;
2010 Nov; 47(11): 977-978
Artigo
em Inglês
| IMSEAR
| ID: sea-168708
ABSTRACT
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.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Idioma:
Inglês
Revista:
Indian Pediatr
Ano de publicação:
2010
Tipo de documento:
Artigo
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