Article
Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology - 1 Aug 2017
Azizi Gholamreza, Abolhassani Hassan, Mahdaviani Seyed Alireza, Chavoshzadeh Zahra, Eshghi Peyman, Yazdani Reza, Kiaee Fatemeh, Shaghaghi Mohammadreza, Mohammadi Javad, Rezaei Nima, Hammarström Lennart, Aghamohammadi Asghar
Abstract excerpt
BACKGROUND: LPS-responsive beige-like anchor protein (LRBA) deficiency is a combined immunodeficiency caused by mutation in LRBA gene. The patients have a variety of clinical symptoms including hypogammaglobulinemia, recurrent infections, autoimmunity, and enteropathy. METHODS: A total of 17 LRBA-deficient patients were enrolled in this longitudinal study. For all patients, demographic information, clinical...
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