Sale!

MT-RNR1 Gene Deafness Nonsyndromic Sensorineural Mitochondrial Genetic Test Cost

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

-21%

The “MT-RNR1 Gene Deafness Nonsyndromic Sensorineural Mitochondrial Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the MT-RNR1 gene, which are associated with nonsyndromic sensorineural deafness. This type of hearing loss is characterized by the impairment of sound transmission from the inner ear to the brain, without other associated systemic findings. The condition is mitochondrial in nature, meaning it is inherited through mutations passed down from the mother, as mitochondria are maternally inherited.

The test is crucial for individuals with a family history of hearing loss or those showing symptoms of sensorineural deafness, as early detection can significantly impact management and treatment options. By analyzing the genetic material for specific mutations in the MT-RNR1 gene, healthcare professionals can provide personalized advice, potential interventions, and family planning guidance to those affected.

DNA Labs UAE offers this genetic testing service at a cost of 4400 AED. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in their state-of-the-art laboratory facilities. The results not only help in confirming the diagnosis but also in understanding the inheritance pattern, which is crucial for affected families. This test represents a blend of advanced genetic science and clinical medicine, aimed at improving the quality of life for individuals with hereditary hearing loss conditions.

Description

MT-RNR1 Gene Deafness Nonsyndromic Sensorineural Mitochondrial Genetic Test

Components: MT-RNR1 Gene Deafness Nonsyndromic Sensorineural Mitochondrial 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: 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 CATSPER13

Test Details: MT-RNR1 gene deafness, nonsyndromic, sensorineural, mitochondrial NGS genetic test is a genetic test that analyzes the MT-RNR1 gene for mutations associated with nonsyndromic sensorineural deafness. Nonsyndromic deafness refers to hearing loss that occurs without any other associated medical conditions or symptoms. Sensorineural deafness specifically refers to hearing loss caused by problems with the inner ear or the auditory nerve pathways. The MT-RNR1 gene, also known as the mitochondrial 12S rRNA gene, is located in the mitochondria, the energy-producing structures within cells. Mutations in this gene have been linked to sensorineural deafness. NGS (Next-Generation Sequencing) technology is used to analyze the MT-RNR1 gene for any genetic variations or mutations. This technique allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic changes associated with deafness. By identifying mutations in the MT-RNR1 gene, this genetic test can help diagnose the genetic cause of nonsyndromic sensorineural deafness and provide valuable information for genetic counseling and potential treatment options.

Test Name	MT-RNR1 Gene Deafness nonsyndromic sensorineural mitochondrial 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 CATSPER13
Test Details	MT-RNR1 gene deafness, nonsyndromic, sensorineural, mitochondrial NGS genetic test is a genetic test that analyzes the MT-RNR1 gene for mutations associated with nonsyndromic sensorineural deafness. Nonsyndromic deafness refers to hearing loss that occurs without any other associated medical conditions or symptoms. Sensorineural deafness specifically refers to hearing loss caused by problems with the inner ear or the auditory nerve pathways. The MT-RNR1 gene, also known as the mitochondrial 12S rRNA gene, is located in the mitochondria, the energy-producing structures within cells. Mutations in this gene have been linked to sensorineural deafness. NGS (Next-Generation Sequencing) technology is used to analyze the MT-RNR1 gene for any genetic variations or mutations. This technique allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic changes associated with deafness. By identifying mutations in the MT-RNR1 gene, this genetic test can help diagnose the genetic cause of nonsyndromic sensorineural deafness and provide valuable information for genetic counseling and potential treatment options.