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Article

FcγRIIa and FcγRIIIa genetic polymorphisms in a group of pediatric immune thrombocytopenic purpura in Egypt.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jan 2012

Eyada Tayseer K, Farawela Hala M, Khorshied Mervat M, Shaheen Iman A, Selim Neama M, Khalifa Iman A S

Abstract excerpt

Immune thrombocytopenic purpura (ITP) is an acquired autoimmune disorder caused by the production of antiplatelet antibodies. The current case-control study aimed at detecting the frequency of FcγRIIa-131H/R and FcγRIIIa-158F/V genes polymorphism in Egyptian children with ITP as genetic markers for ITP risk, and to clear out their possible role in choosing the treatment protocols of ITP. To achieve this aim,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Genetic

Share to Purpura, Thrombocytopenic, Idiopathic

Share to Receptors, IgG

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Source

Identifiers

PMID: 22123287
DOI: 10.1097/MBC.0b013e32834ddf2f

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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