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FGF8 Gene Hypogonadotropic Hypogonadism Type 6 with or without Anosmia Genetic Test Cost

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

-21%

The “FGF8 Gene Hypogonadotropic Hypogonadism Type 6 with or without Anosmia Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE. This test is designed to identify mutations in the FGF8 gene, which are associated with Hypogonadotropic Hypogonadism Type 6, a condition that affects the development and function of the gonads due to insufficient production of gonadotropin-releasing hormone. This can lead to delayed or absent puberty and may be accompanied by anosmia, the inability to perceive odors, depending on the specific genetic mutation present.

The test is priced at 4400 AED and involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab. The sample is then analyzed in the laboratory to detect any genetic alterations in the FGF8 gene that might be responsible for the condition. This genetic test is crucial for the accurate diagnosis and understanding of the individual’s condition, allowing for personalized treatment plans and management strategies to be developed.

By offering this test, DNA Labs UAE provides a vital resource for individuals experiencing symptoms related to Hypogonadotropic Hypogonadism Type 6, enabling them to gain insights into their genetic makeup and how it affects their health. This can also have implications for family planning and the genetic counseling of affected individuals and their families.

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  • This test is not intended for medical diagnosis or treatment
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FGF8 Gene Hypogonadotropic Hypogonadism Type 6 with or without Anosmia Genetic Test

Welcome to DNA Labs UAE, where we offer the FGF8 Gene Hypogonadotropic Hypogonadism Type 6 with or without Anosmia Genetic Test. This test aims to diagnose and provide valuable insights into this specific type of genetic disorder.

Test Details

FGF8 gene hypogonadotropic hypogonadism type 6 with or without anosmia is a genetic disorder that affects the production of sex hormones and the development of reproductive organs. It is caused by mutations in the FGF8 gene, responsible for encoding the fibroblast growth factor 8 protein.

Individuals with this condition may experience delayed or absent puberty, low levels of sex hormones, and infertility. Some may also have a reduced sense of smell (anosmia) due to FGF8’s involvement in the development of the olfactory system.

Test Components and Price

  • Test Name: FGF8 Gene Hypogonadotropic Hypogonadism Type 6 with or without Anosmia 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Before undergoing the FGF8 Gene Hypogonadotropic Hypogonadism Type 6 with or without Anosmia Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by this genetic disorder.

NGS Technology

NGS technology, also known as next-generation sequencing, is a high-throughput method used to analyze multiple genes simultaneously. In the context of hypogonadotropic hypogonadism type 6, NGS genetic testing helps identify mutations in the FGF8 gene, aiding in the diagnosis and treatment decisions. It also provides information about the inheritance pattern of the condition.

Please note that genetic testing should be performed and interpreted by qualified healthcare professionals or genetic counselors who can provide appropriate counseling and guidance based on the results.

Test Name FGF8 Gene Hypogonadotropic hypogonadism type 6 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FGF8 Gene Hypogonadotropic hypogonadism type 6 with or without anosmia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGF8 Gene Hypogonadotropic hypogonadism type 6 with or without anosmia NGS Genetic DNA Test gene FGF8
Test Details

FGF8 gene hypogonadotropic hypogonadism type 6 with or without anosmia is a specific type of genetic disorder that affects the production of sex hormones and the development of reproductive organs. It is caused by mutations in the FGF8 gene, which is responsible for encoding a protein called fibroblast growth factor 8.

This genetic disorder is characterized by delayed or absent puberty, low levels of sex hormones (such as testosterone or estrogen), and infertility. Additionally, some individuals with this condition may also have a reduced sense of smell (anosmia) due to the involvement of FGF8 in the development of the olfactory system.

NGS genetic testing refers to next-generation sequencing, a high-throughput method used to analyze multiple genes simultaneously. In the context of hypogonadotropic hypogonadism type 6, NGS genetic testing can be used to identify mutations in the FGF8 gene that may be causing the disorder. This type of genetic testing can help confirm a diagnosis, guide treatment decisions, and provide information about the inheritance pattern of the condition.

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 results.

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