TACR3 Gene Hypogonadotropic Hypogonadism Type 11 with or without Anosmia Genetic Test
Welcome to DNA Labs UAE, your trusted genetic testing laboratory. Today, we will be discussing the TACR3 Gene Hypogonadotropic Hypogonadism Type 11 with or without Anosmia Genetic Test.
Test Details
The TACR3 gene is associated with a condition called hypogonadotropic hypogonadism type 11 (HH11), which can occur with or without anosmia (the inability to perceive odors). Hypogonadotropic hypogonadism refers to a condition where the production of reproductive hormones, such as luteinizing hormone (LH) and follicle-stimulating hormone (FSH), is reduced. This can lead to delayed or absent puberty, infertility, and other symptoms related to low levels of sex hormones.
NGS genetic testing, or next-generation sequencing genetic testing, is a technique used to analyze multiple genes simultaneously and identify genetic variations that may be associated with a particular condition. In the case of TACR3 gene testing, NGS can be used to identify mutations or variations in the TACR3 gene that may be causing hypogonadotropic hypogonadism type 11. This type of genetic testing can help in confirming a diagnosis, understanding the inheritance pattern of the condition, and providing information for genetic counseling and family planning. It can also be useful for identifying individuals who may benefit from specific treatments or interventions targeted at the underlying genetic cause.
It’s important to note that NGS genetic testing is a specialized test that requires a healthcare professional’s order and interpretation. If you suspect you or someone you know may have hypogonadotropic hypogonadism type 11, it is recommended to consult with a healthcare provider or a genetic counselor to discuss the appropriateness and availability of genetic testing options.
Test Name: TACR3 Gene Hypogonadotropic Hypogonadism Type 11 with or without Anosmia 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 TACR3 Gene Hypogonadotropic Hypogonadism Type 11 with or without Anosmia NGS Genetic DNA Test. A Genetic Counseling session to draw a pedigree chart of family members affected with TACR3 Gene Hypogonadotropic Hypogonadism Type 11 with or without Anosmia NGS Genetic DNA Test gene TACR3.
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Test Name | TACR3 Gene Hypogonadotropic hypogonadism type 11 with or without anosmia 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 TACR3 Gene Hypogonadotropic hypogonadism type 11 with or without anosmia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TACR3 Gene Hypogonadotropic hypogonadism type 11 with or without anosmia NGS Genetic DNA Test gene TACR3 |
Test Details |
The TACR3 gene is associated with a condition called hypogonadotropic hypogonadism type 11 (HH11), which can occur with or without anosmia (the inability to perceive odors). Hypogonadotropic hypogonadism refers to a condition where the production of reproductive hormones, such as luteinizing hormone (LH) and follicle-stimulating hormone (FSH), is reduced. This can lead to delayed or absent puberty, infertility, and other symptoms related to low levels of sex hormones. NGS genetic testing, or next-generation sequencing genetic testing, is a technique used to analyze multiple genes simultaneously and identify genetic variations that may be associated with a particular condition. In the case of TACR3 gene testing, NGS can be used to identify mutations or variations in the TACR3 gene that may be causing hypogonadotropic hypogonadism type 11. This type of genetic testing can help in confirming a diagnosis, understanding the inheritance pattern of the condition, and providing information for genetic counseling and family planning. It can also be useful for identifying individuals who may benefit from specific treatments or interventions targeted at the underlying genetic cause. It’s important to note that NGS genetic testing is a specialized test that requires a healthcare professional’s order and interpretation. If you suspect you or someone you know may have hypogonadotropic hypogonadism type 11, it is recommended to consult with a healthcare provider or a genetic counselor to discuss the appropriateness and availability of genetic testing options. |