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ITM2B Gene Dementia Familial Danish Type Genetic Test Cost

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

-21%

The ITM2B Gene Dementia Familial Danish Type Genetic Test is a specialized diagnostic procedure designed to detect mutations in the ITM2B gene, which are associated with Familial Danish Dementia (FDD). This rare form of dementia is inherited in an autosomal dominant pattern and is characterized by symptoms such as progressive cognitive decline, hearing loss, cataracts, and cerebellar ataxia. The genetic test plays a crucial role in confirming the diagnosis, enabling early intervention and management strategies for affected individuals and their families.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or a cheek swab. The laboratory then analyzes the sample to identify any mutations in the ITM2B gene that are indicative of Familial Danish Dementia. The process is highly accurate and provides vital information for the genetic counseling of families, helping them understand the risk of inheritance and consider future reproductive choices.

The cost of the ITM2B Gene Dementia Familial Danish Type Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of the information it provides for affected families in terms of planning, management, and support cannot be overstated. Early diagnosis through this test can significantly impact the quality of life of individuals with Familial Danish Dementia and their caregivers by allowing for timely interventions and support systems to be put in place.

Description

ITM2B Gene Dementia familial Danish type Genetic Test

At DNA Labs UAE, we offer the ITM2B Gene Dementia familial Danish type Genetic Test. This test is designed to diagnose and identify the genetic cause of dementia, familial, Danish type. Below are the details of the test:

Test Components

Price: 4400.0 AED

Sample Condition

The test requires either a blood sample, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery

The test results will be delivered within 3 to 4 weeks.

Method

The ITM2B Gene Dementia familial Danish type Genetic Test utilizes NGS (Next-Generation Sequencing) technology.

Test Type

This test focuses on neurological disorders, specifically dementia, familial, Danish type.

Doctor

The test is recommended and supervised by a neurologist.

Test Department

The ITM2B Gene Dementia familial Danish type Genetic Test is conducted in our Genetics department.

Pre Test Information

Prior to the test, a genetic counseling session will be conducted to gather clinical history and draw a pedigree chart of affected family members.

Test Details

Dementia, familial, Danish type is a rare genetic disorder caused by mutations in the ITM2B gene. This gene is responsible for producing a protein called amyloid beta peptide, which is found in the brain and plays a role in the development of Alzheimer’s disease. In individuals with dementia, familial, Danish type, mutations in the ITM2B gene lead to the accumulation of amyloid beta peptide in the brain, resulting in the death of brain cells and the onset of dementia.

NGS genetic testing is a cutting-edge method that allows for the analysis of multiple genes simultaneously. This makes it a valuable tool in identifying genetic mutations associated with inherited diseases like dementia, familial, Danish type. If you have a family history of this condition or are experiencing dementia symptoms, your healthcare provider may recommend NGS genetic testing to determine if you have a mutation in the ITM2B gene.

The test involves collecting a sample of your DNA, typically through a blood or saliva sample, and sending it to our laboratory for analysis. The results of the test will assist your healthcare provider in making a diagnosis and developing a personalized treatment plan.

Test Name	ITM2B Gene Dementia familial Danish type Genetic Test
Components
Price	4400.0 AED
Sample Condition	Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery	3 to 4 Weeks
Method	NGS Technology
Test type	Neurological Disorders
Doctor	Neurologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for ITM2B Gene Dementia, familial, Danish type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ITM2B Gene Dementia, familial, Danish type
Test Details	Dementia, familial, Danish type is a rare genetic disorder caused by mutations in the ITM2B gene. This gene provides instructions for making a protein called amyloid beta peptide, which is found in the brain and is involved in the development of Alzheimer’s disease. In people with dementia, familial, Danish type, mutations in the ITM2B gene cause the amyloid beta peptide to accumulate in the brain, leading to the death of brain cells and the development of dementia. NGS genetic testing is a type of genetic test that uses next-generation sequencing technology to analyze a person’s DNA. This technology allows for the analysis of multiple genes at once, making it a useful tool for identifying genetic mutations associated with inherited diseases like dementia, familial, Danish type. If you have a family history of dementia, familial, Danish type, or if you are experiencing symptoms of dementia, your healthcare provider may recommend NGS genetic testing to determine if you have a mutation in the ITM2B gene. This test involves collecting a sample of your DNA, typically through a blood or saliva sample, and sending it to a laboratory for analysis. The results of the test can help your healthcare provider make a diagnosis and develop a treatment plan tailored to your specific needs.

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