Variability of CATCH-22 symptome complex within the framework of 22q11.2 deletion syndrome
Chromosomal pathology is one of the most common causes of congenital malformations. The CATCH-22 symptom complex is most often associated with a microdeletion of chromosome 22, upon detection of which it is customary to diagnose DiGeorge syndrome, a known primary immunodeficiency or syndrome of inna...
| Auteurs principaux: | , , , , , |
|---|---|
| Format: | Article |
| Langue: | Russian |
| Publié: |
St. Petersburg branch of the Russian Association of Allergologists and Clinical Immunologists
2021-12-01
|
| Collection: | Медицинская иммунология |
| Sujets: | |
| Accès en ligne: | https://www.mimmun.ru/mimmun/article/view/2363 |