Clinical Phenotypes of Hyper-IgM Syndromes

The primary immunodeficiency (PID) diseases comprise a heterogeneous group of inherited disorders of immune function. Technical advancements in whole-genome, whole-exome, and RNA-sequencing have seen the explosion of genetic discoveries in the field of PIDs. The present review aims to focus on a gro...

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Veröffentlicht in:	The journal of allergy and clinical immunology in practice (Cambridge, MA) MA), 2016-11, Vol.4 (6), p.1023-1036
1. Verfasser:	de la Morena, M. Teresa, MD
Format:	Artikel
Sprache:	eng
Schlagworte:	Accreditation Algorithms Allergies Allergy and Immunology Antigens Asthma Ataxia Bacterial infections Chronic obstructive pulmonary disease Class switch recombination defects Copyright Cytomegalovirus Defects Deoxyribonucleic acid Disease DNA Gastroesophageal reflux Genetic testing Genotype & phenotype Health education HIGM Humans Hyper-IgM Immunodeficiency Syndrome - genetics Hyper-IgM Immunodeficiency Syndrome - immunology Hyper-IgM syndrome Immunoglobulin Class Switching Immunoglobulin G - immunology Immunoglobulins Immunology Inflammatory bowel disease Internal Medicine Laboratories Microcephaly Phenotype Staphylococcus infections Studies Ulcers XHIGM
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