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NPC1 Gene Niemann-Pick Disease Type C1 Genetic Test

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

-21%

The NPC1 gene Niemann-Pick Disease Type C1 genetic test is a diagnostic tool used to detect mutations in the NPC1 gene, which are responsible for Niemann-Pick disease type C1 (NPC1), a rare and potentially fatal genetic disorder. This condition interferes with the body’s ability to transport and metabolize cholesterol and other fats, leading to their accumulation in various organs, including the liver, spleen, and brain. Symptoms can include difficulty moving, seizures, and cognitive decline, among others, and can vary widely from person to person.

The test involves analyzing the patient’s DNA, extracted from a blood sample, to look for mutations in the NPC1 gene that are known to cause the disease. It is particularly valuable for individuals with a family history of NPC1 or those who exhibit symptoms suggestive of the condition, as early diagnosis can significantly influence management and treatment options.

Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing services, the NPC1 gene test is priced at 4400 AED. DNA Labs UAE employs state-of-the-art technology and highly skilled professionals to ensure accurate and reliable test results, providing crucial information for the diagnosis, treatment planning, and genetic counseling of affected individuals and their families.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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NPC1 Gene Niemann-Pick Disease Type C1 Genetic Test

At DNA Labs UAE, we offer the NPC1 Gene Niemann-Pick Disease Type C1 Genetic Test at a cost of 4400.0 AED.

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

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for NPC1 Gene Niemann-Pick Disease Type C1 NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with NPC1 Gene Niemann-Pick Disease Type C1

Test Details

The NPC1 gene is associated with Niemann-Pick Disease Type C1 (NPC1), a rare genetic disorder characterized by the abnormal accumulation of cholesterol and other lipids in the body’s cells. This accumulation can lead to a variety of symptoms, including progressive neurological deterioration, liver dysfunction, and lung problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the context of NPC1, NGS genetic testing involves sequencing the NPC1 gene to identify any genetic variations or mutations that may be present.

By identifying specific mutations in the NPC1 gene, NGS genetic testing can help confirm a diagnosis of Niemann-Pick Disease Type C1 and provide important information for patient management and genetic counseling. It can also be used for carrier testing in individuals with a family history of the condition.

It’s important to note that NGS genetic testing for NPC1 is typically performed in specialized laboratories and requires a physician’s order. The test results should be interpreted by a healthcare professional with expertise in genetic testing and genetic disorders.

Test Name NPC1 Gene Niemann-Pick disease type C1 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 NPC1 Gene Niemann-Pick disease type C1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NPC1 Gene Niemann-Pick disease type C1
Test Details

The NPC1 gene is associated with Niemann-Pick disease type C1 (NPC1), which is a rare genetic disorder characterized by the abnormal accumulation of cholesterol and other lipids in the body’s cells. This accumulation can lead to a variety of symptoms, including progressive neurological deterioration, liver dysfunction, and lung problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the context of NPC1, NGS genetic testing involves sequencing the NPC1 gene to identify any genetic variations or mutations that may be present.

By identifying specific mutations in the NPC1 gene, NGS genetic testing can help confirm a diagnosis of Niemann-Pick disease type C1 and provide important information for patient management and genetic counseling. It can also be used for carrier testing in individuals with a family history of the condition.

It’s important to note that NGS genetic testing for NPC1 is typically performed in specialized laboratories and requires a physician’s order. The test results should be interpreted by a healthcare professional with expertise in genetic testing and genetic disorders.

SKU: TEST-1870 Category:

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