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Acute intermittent porphyria—another approach to therapy

✍ Scribed by Eva A. Wider de Xifra; Alcira M.del C. Batlle; Ana María Stella; Samuel Malamud

Publisher: Elsevier Science
Year: 1980
Tongue: English
Weight: 473 KB
Volume: 12
Category: Article
ISSN: 0020-711X
DOI: 10.1016/0020-711x(80)90169-x

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## Abstract ## Background Acute intermittent porphyria (AIP) is an autosomal dominant disorder caused by the half‐normal activity of hydroxymethylbilane synthase (HMB‐synthase). Affected individuals can experience episodic, life‐threatening, acute neurological attacks that are precipitated by vari

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