1035

GTD Indications Diagnosis Carrier / Cascade Testing Prenatal GTD Samples Accepted Blood DNA Cultured Cells Amniocyte CVS GTD Test Methodology CNV GTD Methodology Notes Methylation-specific MLPA assay
Generic Test name (cms title) Prader Willi syndrome GTD Test type Single Gene GTD Location Children's Hospital of Eastern Ontario GTD Gene/Platform/Region List 15q11-q13
GTD Category Neurodevelopmental GTD Disease/Condition Prader Willi syndrome (PWS), HHHO (hypogonadism, hypotonia, hypomentia, obesity), Prader-Labhart-Willi syndrome