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CLN5 Gene Ceroid lipofuscinosis neuronal type 5 Genetic Test

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

-21%

The CLN5 gene ceroid lipofuscinosis neuronal type 5 genetic test is a specialized diagnostic tool designed to detect mutations in the CLN5 gene, which are linked to a rare inherited disorder known as neuronal ceroid lipofuscinosis type 5 (NCL5). This condition is part of a group of progressive neurodegenerative diseases that affect the nervous system, leading to symptoms such as vision loss, motor decline, and cognitive impairment. The test is crucial for early diagnosis, enabling timely intervention and management of the disease.

Performed at DNA Labs UAE, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific genetic mutations associated with NCL5. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to accurately interpret the results. By identifying the presence of CLN5 mutations, the test provides essential information for families affected by this condition, facilitating genetic counseling and supporting decisions regarding treatment and care.

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CLN5 Gene Ceroid lipofuscinosis neuronal type 5 Genetic Test

Components: CLN5 Gene Ceroid lipofuscinosis neuronal type 5 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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for CLN5 Gene Ceroid lipofuscinosis neuronal type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Ceroid lipofuscinosis neuronal type 5.

Test Details

The CLN5 gene is associated with a rare genetic disorder called ceroid lipofuscinosis neuronal type 5 (CLN5). This disorder is characterized by the accumulation of lipopigments in various tissues, including the brain, leading to progressive neurodegeneration.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technology to analyze multiple genes simultaneously. In the case of CLN5 gene testing, NGS can be used to identify mutations or variations in the CLN5 gene that may be responsible for the development of ceroid lipofuscinosis neuronal type 5.

NGS genetic testing for CLN5 gene mutations can be helpful in diagnosing individuals suspected of having CLN5-related ceroid lipofuscinosis. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families with a known CLN5 mutation.

By identifying specific mutations in the CLN5 gene, NGS genetic testing can provide valuable information for accurate diagnosis, genetic counseling, and potential treatment options for individuals and families affected by ceroid lipofuscinosis neuronal type 5.

Test Name CLN5 Gene Ceroid lipofuscinosis neuronal type 5 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 CLN5 Gene Ceroid lipofuscinosis neuronal type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Ceroid lipofuscinosis neuronal type 5
Test Details

The CLN5 gene is associated with a rare genetic disorder called ceroid lipofuscinosis neuronal type 5 (CLN5). This disorder is characterized by the accumulation of lipopigments in various tissues, including the brain, leading to progressive neurodegeneration.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technology to analyze multiple genes simultaneously. In the case of CLN5 gene testing, NGS can be used to identify mutations or variations in the CLN5 gene that may be responsible for the development of ceroid lipofuscinosis neuronal type 5.

NGS genetic testing for CLN5 gene mutations can be helpful in diagnosing individuals suspected of having CLN5-related ceroid lipofuscinosis. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families with a known CLN5 mutation.

By identifying specific mutations in the CLN5 gene, NGS genetic testing can provide valuable information for accurate diagnosis, genetic counseling, and potential treatment options for individuals and families affected by ceroid lipofuscinosis neuronal type 5.

SKU: TEST-2211 Category:

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