Systemic lupus erythematosus in a patient with 22q11.2 deletion syndrome: A case report and review of the literature
22q11.2 deletion syndrome (MIM: 192430/188400, ORPHA: 567) is the most common chromosomal microdeletion disorder, caused by a hemizygous microdeletion of 2.5 million base pairs on chromosome 22. There is a known association between 22q11.2 deletion syndrome (22q11.2DS), immunodeficiency and autoimmu...
Saved in:
Main Authors: | Chen Sun, Pingyang Han, Juzhen Yan |
---|---|
Format: | Article |
Language: | English |
Published: |
Termedia Publishing House
2024-11-01
|
Series: | Central European Journal of Immunology |
Subjects: | |
Online Access: | https://www.termedia.pl/Systemic-lupus-erythematosus-in-a-patient-with-22q11-2-deletion-syndrome-A-case-report-and-review-of-the-literature,10,54824,1,1.html |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Treatment of 22q11.2 deletion syndrome-associated schizophrenia with comorbid anxiety and panic disorder
by: Candace B. Borders, et al.
Published: (2017-10-01) -
Characteristics of velopharyngeal dysfunction in 22q11.2 deletion syndrome: a retrospective case-control study
by: Sebastiano Failla, et al.
Published: (2020-07-01) -
Development of Speech and Communication in Polish Children with 22q11.2 Deletion Syndrome: A Cross-Sectional Study
by: Natalia Moćko, et al.
Published: (2024-12-01) -
Driving Innovation to Support Pupils with SEND Through Co-Production in Education and Research: Participatory Action Research with 22q11.2 Deletion Syndrome Families in England
by: Michelle Jayman, et al.
Published: (2024-12-01) -
COVID-19 or systemic lupus erythematosus: Attention to similarity
by: Erden Abdulsamet, et al.
Published: (2025-01-01)