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HGF Gene Deafness Autosomal Recessive Type 39 Genetic Test Cost

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

-21%

The “HGF Gene Deafness Autosomal Recessive Type 39 Genetic Test” is a specialized diagnostic assessment designed to identify mutations in the HGF gene, which are linked to Autosomal Recessive Type 39 Deafness. This condition is a form of genetic hearing loss where an individual must inherit two copies of the altered gene, one from each parent, to be affected. The test is crucial for early detection and management of the condition, allowing for tailored interventions and support.

Performed at DNA Labs UAE, a leading facility in genetic testing, this test provides a comprehensive analysis of the HGF gene to detect any abnormalities that could lead to hearing loss. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately identify mutations in the gene. By opting for this test, individuals at risk can gain valuable insights into their genetic makeup, enabling informed decisions about their health and preventive measures to mitigate the impact of the condition.

Description

HGF Gene Deafness Autosomal Recessive Type 39 Genetic Test

At DNA Labs UAE, we offer the HGF Gene Deafness Autosomal Recessive Type 39 Genetic Test. This test is designed to diagnose a specific type of genetic deafness that is inherited in an autosomal recessive manner. Individuals with this condition must inherit two copies of the mutated HGF gene, one from each parent, in order to develop the condition.

The HGF Gene Deafness Autosomal Recessive Type 39 Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of the HGF gene. This allows us to identify any mutations or variations that may be present. NGS technology is highly accurate and efficient, as it allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of the individual’s genetic makeup.

The cost of the HGF Gene Deafness Autosomal Recessive Type 39 Genetic Test is AED 4400.0. The sample required for this test can be either blood, extracted DNA, or one drop of blood on an FTA card. The report delivery typically takes 3 to 4 weeks.

This test falls under the Ear Nose Throat Disorders category and is conducted by our ENT Doctor in the Genetics department. Before undergoing the test, it is important to provide the clinical history of the patient who is going for the EYA1 Gene Branchiootic Syndrome Type 1 NGS Genetic DNA Test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with the EYA1 Gene Branchiootic Syndrome Type 1 NGS Genetic DNA Test gene EYA9.

The results of the HGF Gene Deafness Autosomal Recessive Type 39 Genetic Test can help confirm a diagnosis of this condition and provide valuable information for genetic counseling, family planning, and potential treatment options.

Test Name	HGF Gene Deafness autosomal recessive type 39 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	Ear Nose Throat Disorders
Doctor	ENT Doctor
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA9
Test Details	HGF Gene Deafness, autosomal recessive type 39 is a specific type of genetic deafness that is inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated HGF gene, one from each parent, in order to develop the condition. To diagnose HGF Gene Deafness, autosomal recessive type 39, a NGS (Next-Generation Sequencing) genetic test can be performed. This test analyzes the DNA sequence of the HGF gene to identify any mutations or variations that may be present. NGS technology allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of the individual’s genetic makeup. It is a highly accurate and efficient method for identifying genetic variations associated with various conditions, including HGF Gene Deafness, autosomal recessive type 39. The results of the NGS genetic test can help in confirming a diagnosis of HGF Gene Deafness, autosomal recessive type 39 and provide valuable information for genetic counseling, family planning, and potential treatment options.