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Article

Low Incidence of α-1 antitrypsin deficiency among babies with prolonged jaundice.

Archives of Iranian medicine - 1 Jan 2013

Jowkar Zahra, Geramizadeh Bita, Fanai Sara, Mirzai Mitra, Dehghani Seyed Mohsen, Haghighat Mahmoud, Honar Naser, Tabei Seyed-Ziyaodin

Abstract excerpt

UNLABELLED: BACKGROUND: α-1 antitrypsin (AAT) deficiency is one of the most important genetic causes of childhood liver diseases in some parts of the world, but its geographic distribution is highly variable. There are many reports from Asian countries such as India, the Philippines, and China which show a very low incidence of this disease. However few studies exist from Iran regarding this genetic deficiency...

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PMID: 23273231
DOI: 013161/AIM.008

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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