Clinical features of acute attacks, chronic symptoms, and long-term complications among patients with acute hepatic porphyria in Japan: a real-world claims database study
Acute hepatic porphyria (AHP) is a family of rare genetic diseases, including acute intermittent porphyria, variegate porphyria, hereditary coproporphyria, and delta-aminolevulinic acid dehydratase-deficient p...
Source: Orphanet Journal of Rare Diseases - Category: Internal Medicine Authors: Yutaka Horie, Yuka Yasuoka and Tomohide Adachi Tags: Research Source Type: research
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