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Article

Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon.

Clinical immunology (Orlando, Fla.) - 1 Oct 2020

Mansour Rana, El-Orfali Youmna, Saber Antoine, Noun Dolly, Youssef Nour, Youssef Yolla, Hanna-Wakim Rima, Dbaibo Ghassan, Abboud Miguel, Massaad Michel J

Abstract excerpt

BACKGROUND: Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency disorder (PID) characterized by microthrombocytopenia, bloody diarrhea, eczema, recurrent infections, and a high incidence of autoimmunity and malignancy. OBJECTIVE: To investigate the mechanism of thrombocytopenia and infections in four boys of consanguineous parents from Lebanon. METHODS: Patient gDNA was studied using Next...

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Identifiers

PMID: 32814211
DOI: 10.1016/j.clim.2020.108573

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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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