Low availability of haematin (hemin) in Pakistan

Madam, Acute Intermittent Porphyria (AIP) is an autosomal dominant disorder that results from a defect in the enzyme named porphobilinogen deaminase.1 It is symptomatic porphyria, involving the accumulation of porphyrins and porphyrin precursors due to impaired conversion in haeme synthesis. Acute...

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Bibliographic Details
Main Authors: Fatima Ahsan, Muhammed Ifham Mohamed Imtiyas, Abdul Raheem Rizvie
Format: Article
Language:English
Published: Pakistan Medical Association 2024-10-01
Series:Journal of the Pakistan Medical Association
Subjects:
Online Access:https://jpma.org.pk/index.php/public_html/article/view/10726
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