Common variable immunodeficiency in a patient with Noonan syndrome
Noonan syndrome is a disease that occurs in 1 in 1,000–2,500 live births, mostly inherited in an autosomal dominant manner. Noonan syndrome is a clinically and genetically heterogeneous disease that may be accompanied by growth retardation, prominent facial dysmorphic features, congenital heart defe...
Saved in:
| Main Authors: | , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Termedia Publishing House
2024-11-01
|
| Series: | Alergologia Polska |
| Subjects: | |
| Online Access: | https://www.termedia.pl/Common-variable-immunodeficiency-in-a-patient-with-Noonan-syndrome,123,55108,1,1.html |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|