학술논문
Severe combined immunodeficiency.
Document Type
Article
Author
Source
Australian Doctor; 3/3/2023, p19-26, 6p
Subject
Language
ISSN
10397116
Abstract
The article discusses about initial pathway to diagnosis and referral pathways in the treatment of severe combined immunodeficiency (SCID), a group of about 20 rare inherited syndromes caused by genetic defects that impact normal T-cell and B-cell function. Topics discussed include errors of immunity in genes, newborn screening in Australia for SCID and SCID in the absence of genetic cause.