22 q11 microdeletion syndrome is a birth defect caused by a genetic abnormality that occurs in approximately one in 700 births.
Also variously nicknamed, or labelled according to symptomatic manifestations:
- Catch 22
- Conotruncal face anomaly
- Craniofacial syndrome
- DiGeorge syndrome
- Shprintzen syndrome
- Unusual face syndrome
- Velocardio-facial syndrome (VCFS)
1. Cardiac Manifestations
CLINICAL FEATURES:
This is a partial list among a great variety of problems associated with VCFS. None of these features occur in 100% of cases.
2. Facial Manifestations
3. Endocrine Manifestations
4. Immune Manifestations
5. Other Manifestations
See also: Reelin hypothesis of the development of Schizophrenia (speculative)
External links