GPR161 Gene Pituitary Stalk Interruption Syndrome Genetic Test
Welcome to DNA Labs UAE, where we offer the GPR161 Gene Pituitary Stalk Interruption Syndrome genetic test. This test can help diagnose and identify mutations associated with this rare genetic disorder.
Test Details
The GPR161 gene, also known as G protein-coupled receptor 161, plays a crucial role in the development and functioning of the pituitary gland. Mutations in this gene have been linked to a rare genetic disorder called Pituitary Stalk Interruption Syndrome (PSIS).
PSIS is characterized by the absence or underdevelopment of the pituitary stalk, which connects the hypothalamus to the pituitary gland. This disruption can result in hormonal deficiencies and various symptoms, including growth hormone deficiency, hypothyroidism, adrenal insufficiency, and reproductive problems.
To diagnose PSIS and identify GPR161 mutations, we utilize a genetic test called Next-Generation Sequencing (NGS) technology. NGS allows for the simultaneous analysis of multiple genes, including GPR161. This test involves sequencing the DNA of an individual to identify any mutations or variations in the GPR161 gene that may be associated with PSIS.
Test Components
- Test Name: GPR161 Gene Pituitary Stalk Interruption Syndrome GPR161 related Genetic Test
- 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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
- Pre Test Information: Clinical History of Patient who is going for GPR161 Gene Pituitary stalk interruption syndrome, GPR161 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Pituitary stalk interruption syndrome, GPR161 related.
Benefits of Genetic Testing
NGS genetic testing for GPR161-related disorders can provide several benefits, including:
- Confirmation of diagnosis
- Guidance for treatment decisions
- Information about the risk of passing the condition on to future generations
It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support.
At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. If you suspect PSIS or have a family history of the disorder, our GPR161 Gene Pituitary Stalk Interruption Syndrome genetic test can provide valuable insights. Contact us today to learn more or schedule an appointment.
Test Name | GPR161 Gene Pituitary stalk interruption syndrome GPR161 related 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 | Metabolic Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for GPR161 Gene Pituitary stalk interruption syndrome, GPR161 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Pituitary stalk interruption syndrome, GPR161 related |
Test Details |
GPR161, also known as G protein-coupled receptor 161, is a gene that plays a role in the development and functioning of the pituitary gland. Mutations in this gene have been associated with a rare genetic disorder called pituitary stalk interruption syndrome (PSIS). PSIS is characterized by the absence or underdevelopment of the pituitary stalk, which connects the hypothalamus to the pituitary gland. This disruption can lead to hormonal deficiencies and various symptoms, including growth hormone deficiency, hypothyroidism, adrenal insufficiency, and reproductive problems. To diagnose PSIS and identify GPR161 mutations, a genetic test called next-generation sequencing (NGS) can be performed. NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes, including GPR161. This test involves sequencing the DNA of an individual to identify any mutations or variations in the GPR161 gene that may be associated with PSIS. NGS genetic testing for GPR161-related disorders can help confirm a diagnosis, guide treatment decisions, and provide information about the risk of passing the condition on to future generations. It is typically recommended for individuals with suspected PSIS or a family history of the disorder. It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support. |