Velocardiofacial syndrome

A chromosomal disease that has material basis in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features.

Also known as: 22q11 deletion syndrome, Shprintzen VCF syndrome, VCF syndrome, deletion 22q11.2 syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22Q11.2 deletion syndrome

4 clinical trials for this condition and its sub-types, 4 tagged with Velocardiofacial syndrome itself.