A Novel Variant of CORO1A Gene Contributing to The Development of Primary Immunodeficiency in Children
Abstract
The case report describes a novel finding of a homozygous variant in the CORO1A gene, associated with severe combined immunodeficiency (SCID), in a 9-year-old female patient with recurrent infections and unique immunological features, including T-cell lymphocytosis and B-cell lymphopenia.
Fields of Study & Subjects
Immunodeficiency and Autoimmune Disorders
T-cell and B-cell Immunology
Blood disorders and treatments
Publication details
- Journal / source
- World Allergy Organization Journal
- Publisher
- Elsevier BV
- Volume
- 19
- Issue
- 2
- Pages
- 101258–101258
- Publication date
- 1 February 2026
- Language
- EN