B Cell Disorders in Children: Part II.

Abstract:

PURPOSE OF REVIEW:B cell disorders result in decreased levels or function of immunoglobulins in an individual. Genetic mutations have been reported in a variety of B cell disorders. This review, in follow-up to a previous review, describes some rare B cell disorders as well as their known underlying genetic etiologies. RECENT FINDINGS:Genetic studies identify and permit precise classification of an increasing number of B cell disorders, leading to a greater understanding of B cell development and function. The B cell disorders are rare diseases. While clinicians are most familiar with X-linked agammaglobulinemia and so-called common variable immunodeficiency (CVID), there are many causes of hypogammaglobulinemia. Genetic testing provides a specific diagnosis, offers useful information for genetic counseling, and can identify previously unrecognized B cell disorders.

authors

Griffin DD,Dolen WK

doi

10.1007/s11882-020-00963-z

subject

Has Abstract

pub_date

2020-08-21 00:00:00

pages

64

issue

11

eissn

1529-7322

issn

1534-6315

pii

10.1007/s11882-020-00963-z

journal_volume

20

pub_type

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