Congenital adrenal hyperplasia
Analysis ID 108
Analysis location “GENESIS” Centre for Medical Genetics
Diagnosed illness Congenital adrenal hyperplasia
OMIM +201910
Clinical information Analysis of seven most common mutations in the 21-α-hydroxylase gene
Type of analysis molecular
Type of biological material 5 ml peripheral blood collected in the EDTA tube
Analyzed genes CYP21A
Analysis description
Analysis indication Symptoms of congenital adrenal hyperplasia
Analysis time To be adjusted individually
Refund Yes
CGM laboratory name Laboratory for diagnostics of the hereditary disorders