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ESRRB Gene Deafness Autosomal Recessive Type 35 Genetic Test

Name: ESRRB Gene Deafness Autosomal Recessive Type 35 Genetic Test
SKU: TEST-2718
Price: 4400 AED
Availability: InStock

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

-21%

The ESRRB Gene Deafness Autosomal Recessive Type 35 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the ESRRB gene that are responsible for Autosomal Recessive Deafness Type 35 (DFNB35). This condition is characterized by non-syndromic sensorineural hearing loss, which means it affects the inner ear or the nerve pathways to the brain without affecting other parts of the body. The test is crucial for families with a history of this condition, as it can provide definitive diagnosis, inform treatment decisions, and guide family planning.

Conducted through a sample of blood or saliva, the test specifically looks for alterations in the ESRRB gene, which plays a significant role in the development and maintenance of inner ear structures essential for hearing. Identifying a mutation can help in understanding the cause of deafness in an individual or family, facilitating early intervention and management strategies.

The cost of the ESRRB Gene Deafness Autosomal Recessive Type 35 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately detect and interpret genetic mutations associated with this form of hearing loss.

Description

ESRRB Gene Deafness Autosomal Recessive Type 35 Genetic Test

Test Name: ESRRB Gene Deafness Autosomal Recessive Type 35 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER9

Test Details: The ESRRB gene is associated with deafness, specifically autosomal recessive type 35 (DFNB35). Autosomal recessive inheritance means that an individual must inherit two copies of the mutated gene, one from each parent, in order to develop the condition. NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the simultaneous analysis of multiple genes or the entire genome. In the case of ESRRB gene deafness, an NGS genetic test would involve sequencing the ESRRB gene to identify any mutations or variants that may be responsible for the condition. This type of genetic testing can help diagnose individuals with DFNB35 and provide information about the underlying genetic cause of their deafness. It can also be used for carrier testing, which can help determine if individuals are carriers of the ESRRB gene mutation and may pass it on to their children. It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.

Test Name	ESRRB Gene Deafness autosomal recessive type 35 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 CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CATSPER2 Gene Deafness and male infertility, CATSPER2 related NGS Genetic DNA Test gene CATSPER9
Test Details	The ESRRB gene is associated with deafness, specifically autosomal recessive type 35 (DFNB35). Autosomal recessive inheritance means that an individual must inherit two copies of the mutated gene, one from each parent, in order to develop the condition. NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the simultaneous analysis of multiple genes or the entire genome. In the case of ESRRB gene deafness, an NGS genetic test would involve sequencing the ESRRB gene to identify any mutations or variants that may be responsible for the condition. This type of genetic testing can help diagnose individuals with DFNB35 and provide information about the underlying genetic cause of their deafness. It can also be used for carrier testing, which can help determine if individuals are carriers of the ESRRB gene mutation and may pass it on to their children. It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.