4019

GTD Indications Diagnosis Carrier / Cascade Testing GTD Samples Accepted Blood GTD Test Methodology FISH GTD Methodology Notes Constitutional FISH
GTD Notes Before requesting this test, please contact the lab for information regarding eligibility and availability of testing for your patient. Generic Test name (cms title) FISH: 22q11.21 Deletion Syndrome GTD Test type Cytogenetic GTD Location London Health Sciences Centre GTD Gene/Platform/Region List HIRA
GTD Category Chromosomal Anomalies GTD Disease/Condition DiGeorge (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))