1008

GTD Indications Carrier / Cascade Testing Diagnosis Prenatal GTD Samples Accepted Amniocyte Blood CVS Generic Test name (cms title) 22q11.21 Deletion Syndrome GTD Test type Cytogenetic GTD Gene/Platform/Region List HIRA (TUPLE1), 22q11.21
GTD Category Chromosomal Anomalies GTD Disease/Condition 22q11.21 Deletion Syndrome (DiGeorge syndrome (DGS), velocardiofacial syndrome (VCFS), conotruncal anomaly face syndrome (CTAF), Opitz G/BBB syndrome, and Cayler cardiofacial syndrome (asymmetric crying facies), Sedlackova syndrome, Shprintzen Syndrome)