| Literature DB >> 30610030 |
Corrado Campochiaro1, Sirin Atay1, Kristina E N Clark1, Voon Ong2, Christopher P Denton2.
Abstract
Selective immunoglobulin M deficiency (sIgMD) is an immunodeficiency with undefined pathogenesis and commonly presenting with recurrent infections. 1 The European Society for Immunodeficiencies Registry defines sIgMD as a serum IgM level repeatedly below 2 SD of normal with normal levels of serum IgA, IgG and IgG subclasses, normal vaccination responses, absence of T-cell defects and absence of causative external factors. Rarely it can also be associated with autoimmune diseases. 2-7 Here we describe a patient with primary sIgMD; who presented with multiple autoimmune diseases without a history of recurrent infections and we provide a short literature review on sIgMD and autoimmune diseases. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: connective tissue disease; immunology
Mesh:
Substances:
Year: 2019 PMID: 30610030 PMCID: PMC6326303 DOI: 10.1136/bcr-2017-223180
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X