Disorders of Sexual Development Panel (10 Genes)

Clinical Research Prenatal Carrier

Test Details
Disorder◦ 17-Beta Hydroxysteroid Dehydrogenase III Deficiency
◦ Androgen Insensitivity Syndrome
◦ Aromatase Deficiency
◦ Complete Androgen Insensitivity Syndrome
◦ Partial Androgen Insensitivity Syndrome
◦ SRY-Related 46,XY DSD and 46,XY CGD
◦ Steroid 5-Alpha-Reductase Deficiency
Type◦ Molecular
◦ Multi-Gene Panel
Method◦ Del/Dup (CNV)
◦ Mutation Scanning of Entire Coding Region
◦ Sequencing, Next Gen
GenesAR, CYP17A1, CYP19A1, HSD17B3, LHCGR, NR5A1, POR, SRD5A2, SRY, WT1
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EvolveGene
12105 28th St N, Suite A
St. Petersburg
FL 33716
USA

email: adam.coovadia@evolvegene.com

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