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Gene Analysis Smith-Lemli-Opitz Syndrome (DHCR7)
Gene Analysis Smith-Lemli-Opitz Syndrome (DHCR7) identifies mutations in the DHCR7 gene, associated with Smith-Lemli-Opitz syndrome, a genetic disorder that causes developmental delay, congenital malformations, and intellectual disability.
13 days
Report Ready
No Fasting
Fasting
5-99
Age Group
Home
Collection
Preparation
Why this test
Fasting Required
Not Required
⏱ Report Time
13 days
🧫 Sample Type
Blood
🎂 Age Group
5-99
👤 Gender
Male,Female
🏠 Collection
Home Visit
Gene Analysis Smith-Lemli-Opitz Syndrome (DHCR7)
Gene Analysis Smith-Lemli-Opitz Syndrome (DHCR7)
