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CISD2 Gene Wolfram Syndrome Type 2 Genetic Test Cost

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

-21%

The CISD2 Gene Wolfram Syndrome Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the CISD2 gene that are associated with Wolfram Syndrome Type 2. This rare genetic disorder is characterized by diabetes mellitus, optic atrophy, and deafness, among other symptoms. Early and accurate detection through this test can aid in the management and treatment of the condition. The test is priced at 4400 AED and involves analyzing the patient’s DNA to identify any genetic variations that may indicate the presence of the syndrome. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test is crucial for individuals with a family history of Wolfram Syndrome Type 2 or those exhibiting symptoms related to the disorder, providing them with valuable insights into their genetic health.

Description

CISD2 Gene Wolfram Syndrome Type 2 Genetic Test

Test Name: CISD2 Gene Wolfram syndrome type 2 Genetic Test

Components: DNA Labs UAE offers the CISD2 Gene Wolfram syndrome type 2 Genetic Test at a price of 4400.0 AED.

Sample Condition: The test can be conducted using blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery: The test results are typically delivered within 3 to 4 weeks.

Method: The test utilizes NGS (Next-Generation Sequencing) technology.

Test Type: The test is specifically designed to detect Ear Nose Throat Disorders.

Doctor: The test is conducted by an ENT Doctor.

Test Department: The test is conducted in the Genetics department.

Pre Test Information: Before conducting the CISD2 Gene Wolfram syndrome type 2 Genetic Test, it is important to gather the clinical history of the patient. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by the EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA20.

Test Details: The CISD2 gene is associated with Wolfram syndrome type 2, a rare genetic disorder characterized by the development of diabetes mellitus and optic atrophy. This syndrome is caused by mutations in the CISD2 gene, which plays a role in regulating cellular processes such as mitochondrial function and calcium homeostasis. The NGS genetic testing technique is used to analyze multiple genes simultaneously and identify mutations or variations in the DNA sequence. In the context of Wolfram syndrome type 2, the NGS genetic test can detect mutations in the CISD2 gene, aiding in the diagnosis confirmation and providing genetic counseling to affected individuals and their families. The test involves obtaining a blood or saliva sample, extracting the DNA, and sequencing it using NGS technology. The resulting DNA sequence data is then analyzed to identify any mutations or variations associated with the disorder. It is crucial to have the test performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Test Name	CISD2 Gene Wolfram syndrome type 2 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 EYA20
Test Details	The CISD2 gene is associated with Wolfram syndrome type 2, which is a rare genetic disorder characterized by the development of diabetes mellitus and optic atrophy. Wolfram syndrome type 2 is caused by mutations in the CISD2 gene, which is involved in regulating cellular processes such as mitochondrial function and calcium homeostasis. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and detect mutations or variations in the DNA sequence. In the context of Wolfram syndrome type 2, NGS genetic testing can be used to identify mutations in the CISD2 gene, helping to confirm a diagnosis and provide genetic counseling to affected individuals and their families. The NGS genetic test for Wolfram syndrome type 2 typically involves obtaining a blood or saliva sample from the individual being tested. The DNA is then extracted from the sample and sequenced using NGS technology. The resulting DNA sequence data is analyzed to identify any mutations or variations in the CISD2 gene that may be associated with the disorder. It is important to note that genetic testing for Wolfram syndrome type 2 should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.