DiGeorge II, (FISH)
On demand
Order number :
CO-F06
DiGeorge II microdeletion
Main indication:
10p14 deletion detection.
Test usage:
Analysis by Fluorescence In Situ Hybridization (FISH) is available for a wide range of microdeletion syndromes. This is a rare genetic syndrome characterized by facial anomalies, congenital heart defects, T-cell immune defects, hypoparathyroid/ hypocalcemia and mental retardation. DGS2 is associated with a partial deletion of the short arm of chromosome 10. Patients with this deletion have many of the same conditions as patients with DGS1 del 22q11.2.