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FSHR Gene Ovarian dysgenesis type 1 Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The FSHR Gene Ovarian Dysgenesis Type 1 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the FSHR gene, which are linked to Ovarian Dysgenesis Type 1. This condition is a form of primary ovarian insufficiency, where the ovaries do not develop properly, leading to issues with fertility and potentially causing early menopause among affected women. The FSHR gene plays a crucial role in the reproductive system, particularly in the development and function of the ovaries. Mutations in this gene can disrupt normal ovarian development and function, making this test crucial for early diagnosis and management of the condition.

Priced at 4400 AED, the test provides individuals and families with critical information regarding genetic predispositions that could affect ovarian health and fertility. Conducted at DNA Labs UAE, a facility renowned for its cutting-edge technology and expertise in genetic diagnostics, this test is a valuable resource for those seeking to understand their reproductive health better. Early detection through this genetic testing can facilitate timely interventions and informed decisions regarding fertility planning and management, enhancing the quality of life for those affected by Ovarian Dysgenesis Type 1.

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Test Name FSHR Gene Ovarian dysgenesis type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Reproductive Disorders
Doctor Gynecology
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FSHR Gene Ovarian dysgenesis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FSHR Gene Ovarian dysgenesis type 1 NGS Genetic DNA Test gene FSHR
Test Details

The FSHR gene is responsible for encoding the follicle-stimulating hormone receptor, which plays a crucial role in the reproductive system. Ovarian dysgenesis type 1 is a condition characterized by the underdevelopment or absence of ovarian tissue, leading to infertility and other reproductive issues in affected individuals.

NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze DNA or RNA sequences. In the context of ovarian dysgenesis type 1, NGS genetic testing can be used to identify mutations or variations in the FSHR gene that may be associated with the condition. This type of testing can help diagnose individuals with ovarian dysgenesis type 1 and provide valuable information for genetic counseling and family planning.

During the NGS genetic testing process, a DNA sample is obtained from the individual being tested, usually through a blood sample. The DNA is then sequenced using advanced technologies, allowing for the detection of variations in the FSHR gene. The obtained sequence data is then analyzed and compared to reference sequences to identify any potential disease-causing mutations or variations.

NGS genetic testing for ovarian dysgenesis type 1 can provide important insights into the genetic basis of the condition and help guide treatment options and reproductive planning for affected individuals and their families. It is typically performed by specialized genetic testing laboratories and may require a healthcare provider’s referral.

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