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INHBA Gene FSH Releasing Protein Deficiency Genetic Test Cost

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

-21%

The INHBA Gene FSH Releasing Protein Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect deficiencies in the protein responsible for the release of follicle-stimulating hormone (FSH) due to mutations in the INHBA gene. This gene plays a critical role in reproductive biology, influencing fertility and various hormonal functions. A deficiency can lead to reproductive issues and hormonal imbalances, making this test crucial for individuals experiencing related symptoms or those with a family history of fertility issues. The test, priced at 4400 AED, involves a comprehensive analysis of the INHBA gene to identify any mutations that may be affecting FSH production. Conducted in the state-of-the-art facilities of DNA Labs UAE, it provides valuable insights for personalized treatment plans and informed family planning decisions.

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INHBA Gene FSH releasing protein deficiency Genetic Test

Welcome to DNA Labs UAE, where we offer the INHBA Gene FSH releasing protein deficiency Genetic Test. This test helps in diagnosing and understanding the causes of FSH releasing protein deficiency, a condition related to the INHBA gene. Read on to learn more about the test details, symptoms, diagnosis, and cost.

Test Name: INHBA Gene FSH releasing protein deficiency 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: Hepatology Nephrology Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information

Prior to undergoing the INHBA Gene FSH releasing protein deficiency NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by INHBA Gene FSH releasing protein deficiency.

Test Details

The INHBA gene is responsible for encoding the inhibin beta A subunit, which plays a crucial role in the production of inhibin. Inhibin is a hormone that regulates the secretion of follicle-stimulating hormone (FSH) in the pituitary gland. FSH releasing protein deficiency occurs when there is a lack of inhibin, resulting in increased FSH levels. This condition can lead to various reproductive abnormalities, including infertility, menstrual irregularities, and early onset of menopause.

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously using advanced sequencing technologies. This allows for the detection of genetic variations, such as mutations or changes in the INHBA gene, which may be responsible for FSH releasing protein deficiency. By performing an NGS genetic test, healthcare providers can identify specific genetic variations that contribute to the condition, enabling them to provide a more accurate diagnosis and personalized treatment options for affected individuals.

If you suspect that you or a family member may have FSH releasing protein deficiency, we recommend considering the INHBA Gene FSH releasing protein deficiency Genetic Test. Early diagnosis and personalized treatment can make a significant difference in managing the condition and improving quality of life.

Test Name INHBA Gene FSH releasing protein deficiency 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for INHBA Gene FSH releasing protein deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with INHBA Gene FSH releasing protein deficiency NGS Genetic DNA Test gene INHBA
Test Details

The INHBA gene encodes for the inhibin beta A subunit, which is involved in the production of inhibin, a hormone that regulates the secretion of follicle-stimulating hormone (FSH) in the pituitary gland.

FSH releasing protein deficiency is a condition characterized by a lack of inhibin, leading to increased FSH levels. This can result in various reproductive abnormalities, such as infertility, menstrual irregularities, and early onset of menopause.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that analyzes multiple genes simultaneously using advanced sequencing technologies. It allows for the detection of genetic variations, including mutations or changes in the INHBA gene, which may be responsible for FSH releasing protein deficiency.

By performing an NGS genetic test, healthcare providers can identify specific genetic variations that may be contributing to the condition, enabling them to provide a more accurate diagnosis and personalized treatment options for affected individuals.