Sale!

SEMA3A Gene Kallmann Syndrome SEMA3A Related Genetic Test Cost

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

-21%

The SEMA3A gene plays a crucial role in the development of the nervous system and has been linked to Kallmann Syndrome, a genetic condition characterized by the failure to start or fully complete puberty, combined with an impaired sense of smell (anosmia). This condition results from the abnormal development of certain neurons that are essential for the release of sex hormones. Mutations in the SEMA3A gene disrupt the normal signaling pathways necessary for neuronal development, leading to the symptoms observed in Kallmann Syndrome.

To diagnose and confirm the presence of SEMA3A-related Kallmann Syndrome, genetic testing is available at DNA Labs UAE. This specialized test involves analyzing the patient’s DNA to identify mutations in the SEMA3A gene that are known to cause the condition. The process is comprehensive, ensuring accurate diagnosis which is crucial for the management and treatment of the syndrome.

The cost of the SEMA3A related genetic test at DNA Labs UAE is 4400 AED. This test is a valuable tool for individuals with a clinical diagnosis or symptoms suggestive of Kallmann Syndrome, as well as for family members of affected individuals who may be at risk. Early and accurate diagnosis through genetic testing can significantly improve the quality of life for those affected by providing appropriate treatment options and genetic counseling.

Description

SEMA3A Gene Kallmann syndrome SEMA3A related Genetic Test

Test Name: SEMA3A Gene Kallmann syndrome SEMA3A related Genetic Test

Components: SEMA3A gene

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 SEMA3A Gene Kallmann syndrome, SEMA3A related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SEMA3A Gene Kallmann syndrome, SEMA3A related NGS Genetic DNA Test gene SEMA3A

Test Details:

SEMA3A gene is associated with Kallmann syndrome, a genetic disorder characterized by delayed or absent puberty and an impaired sense of smell. The SEMA3A gene provides instructions for making a protein called semaphorin 3A, which is involved in the development of neurons and the formation of nerve connections.

A SEMA3A-related next-generation sequencing (NGS) genetic test is a diagnostic tool used to identify mutations or variations in the SEMA3A gene. This test involves sequencing the DNA of an individual to analyze the specific sequence of the SEMA3A gene and identify any genetic changes that may be present.

By detecting mutations or variations in the SEMA3A gene, this NGS genetic test can help confirm a diagnosis of Kallmann syndrome and provide valuable information for genetic counseling and family planning. It can also aid in the understanding of the underlying genetic causes of the disorder and potentially guide treatment decisions.

It is important to note that this genetic test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and guidance based on the test results.

Test Name	SEMA3A Gene Kallmann syndrome SEMA3A 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	Hepatology Nephrology Endocrinology Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for SEMA3A Gene Kallmann syndrome, SEMA3A related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SEMA3A Gene Kallmann syndrome, SEMA3A related NGS Genetic DNA Test gene SEMA3A
Test Details	SEMA3A gene is associated with Kallmann syndrome, a genetic disorder characterized by delayed or absent puberty and an impaired sense of smell. The SEMA3A gene provides instructions for making a protein called semaphorin 3A, which is involved in the development of neurons and the formation of nerve connections. A SEMA3A-related next-generation sequencing (NGS) genetic test is a diagnostic tool used to identify mutations or variations in the SEMA3A gene. This test involves sequencing the DNA of an individual to analyze the specific sequence of the SEMA3A gene and identify any genetic changes that may be present. By detecting mutations or variations in the SEMA3A gene, this NGS genetic test can help confirm a diagnosis of Kallmann syndrome and provide valuable information for genetic counseling and family planning. It can also aid in the understanding of the underlying genetic causes of the disorder and potentially guide treatment decisions. It is important to note that this genetic test should be ordered and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate counseling and guidance based on the test results.