Acute intermittent porphyria with transient cortical blindness.
نویسندگان
چکیده
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.
منابع مشابه
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عنوان ژورنال:
- Indian pediatrics
دوره 47 11 شماره
صفحات -
تاریخ انتشار 2010