PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia Genetic Test
At DNA Labs UAE, we offer the PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia Genetic Test. This test is designed to diagnose and identify the genetic factors associated with hypogonadotropic hypogonadism type 3 (HH3), a condition characterized by a deficiency in the production or release of hormones necessary for normal sexual development and reproduction.
Test Components
- PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia Genetic Test
Price
The cost of the PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia Genetic Test is AED 4400.0.
Sample Condition
The sample required for this test can be either blood, extracted DNA, or one drop of blood on an FTA card.
Report Delivery
The report for the PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia Genetic Test will be delivered within 3 to 4 weeks.
Method
The test is performed using NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes.
Test Type
The PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia Genetic Test falls under the category of Hepatology, Nephrology, and Endocrinology Disorders.
Doctor
This test can be ordered by a General Physician.
Test Department
The PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia Genetic Test is conducted in the Genetics department.
Pre Test Information
Prior to undergoing the PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by the condition.
Test Details
The PROKR2 gene is associated with hypogonadotropic hypogonadism type 3 (HH3), which can occur with or without anosmia (the inability to smell). NGS genetic testing is used to analyze multiple genes simultaneously and can identify any mutations or variations in the PROKR2 gene that may be responsible for the development of HH3. This test is helpful in confirming a diagnosis of HH3, especially in individuals experiencing delayed puberty, infertility, and reduced or absent sense of smell. It is also beneficial for genetic counseling and family planning purposes. It is crucial to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and guidance based on the test results.
| Test Name | PROKR2 Gene Hypogonadotropic hypogonadism type 3 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 PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PROKR2 Gene Hypogonadotropic hypogonadism type 3 with or without anosmia NGS Genetic DNA Test gene PROKR2 |
| Test Details |
The PROKR2 gene is associated with a condition called hypogonadotropic hypogonadism type 3 (HH3), which can occur with or without anosmia (the inability to smell). HH3 is a form of hypogonadotropic hypogonadism, which is characterized by a deficiency in the production or release of hormones that are necessary for normal sexual development and reproduction. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PROKR2 gene testing, NGS can be used to identify any mutations or variations in the gene that may be responsible for the development of HH3. Genetic testing for PROKR2 gene mutations can be helpful in confirming a diagnosis of HH3, especially in individuals who exhibit symptoms such as delayed puberty, infertility, and reduced or absent sense of smell. It can also be useful for genetic counseling and family planning purposes. It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate counseling and guidance based on the test results. |
