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ECM1 Gene Urbach-Wiethe disease Genetic Test Cost

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

-21%

The ECM1 gene Urbach-Wiethe disease genetic test is a specialized diagnostic tool used to identify mutations in the ECM1 gene, which are associated with Urbach-Wiethe disease (UWD), a rare genetic disorder. This condition is characterized by a variety of symptoms, including skin thickening, hoarseness of voice, and, in some cases, neurological issues due to calcium deposits in the brain. The ECM1 gene plays a critical role in skin integrity and structure, and mutations in this gene can lead to the hallmark features of UWD.

The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in a laboratory to identify any genetic abnormalities in the ECM1 gene. This genetic test is crucial for the accurate diagnosis of Urbach-Wiethe disease, enabling healthcare providers to offer appropriate management and treatment options for affected individuals.

The ECM1 gene Urbach-Wiethe disease genetic test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, reflecting the specialized nature of the testing and the expertise required to interpret the results. By offering this test, DNA Labs UAE provides an essential service for patients and families affected by Urbach-Wiethe disease, facilitating early diagnosis and intervention for this rare genetic condition.

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  • This test is not intended for medical diagnosis or treatment
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ECM1 Gene Urbach-Wiethe disease 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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for ECM1 Gene Urbach-Wiethe disease NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with Urbach-Wiethe disease

Test Details

ECM1 gene is associated with a rare genetic disorder called Urbach-Wiethe disease, also known as lipoid proteinosis. This disease is characterized by the accumulation of a protein-like substance called hyaline in various tissues and organs of the body.

Next-generation sequencing (NGS) is a genetic testing method that allows the simultaneous sequencing of multiple genes or even the entire genome. In the case of Urbach-Wiethe disease, NGS can be used to analyze the ECM1 gene for any genetic mutations or variations that may be responsible for causing the disease.

By performing an NGS genetic test on the ECM1 gene, healthcare professionals can identify specific mutations or variations that may be present in an individual’s DNA. This information can help in diagnosing Urbach-Wiethe disease and understanding its genetic basis.

NGS genetic testing can also be used for carrier screening, prenatal testing, and predicting the risk of developing certain genetic disorders. It provides a comprehensive and efficient approach to genetic testing, allowing for the analysis of multiple genes simultaneously and providing more detailed information about an individual’s genetic makeup.

Test Name ECM1 Gene Urbach-Wiethe disease 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ECM1 Gene Urbach-Wiethe disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Urbach-Wiethe disease
Test Details

ECM1 gene is associated with a rare genetic disorder called Urbach-Wiethe disease, also known as lipoid proteinosis. This disease is characterized by the accumulation of a protein-like substance called hyaline in various tissues and organs of the body.

Next-generation sequencing (NGS) is a genetic testing method that allows the simultaneous sequencing of multiple genes or even the entire genome. In the case of Urbach-Wiethe disease, NGS can be used to analyze the ECM1 gene for any genetic mutations or variations that may be responsible for causing the disease.

By performing an NGS genetic test on the ECM1 gene, healthcare professionals can identify specific mutations or variations that may be present in an individual’s DNA. This information can help in diagnosing Urbach-Wiethe disease and understanding its genetic basis.

NGS genetic testing can also be used for carrier screening, prenatal testing, and predicting the risk of developing certain genetic disorders. It provides a comprehensive and efficient approach to genetic testing, allowing for the analysis of multiple genes simultaneously and providing more detailed information about an individual’s genetic makeup.

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