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Niemann-Pick Disease Gene Panel Test
Also known as: Niemann - Pick Disease Gene Panel by NGS, EDTA Blood**
No special precautions
Sample Type
Blood
Recommended for
Male, Female
Blood test at Home
NABL & CAP Accredited Labs
Accurate & Quality Test Reports
Trusted by Leading Doctors & Hospitals
Overview
Specific genes are associated with Niemann-Pick disease. This genetic disorder affects the body's ability to process lipids correctly, leading to an abnormal buildup and storage of these fats within cells. Understanding the genetic mutations involved can help in diagnosing and managing the disease effectively
Niemann - Pick Disease Gene Panel by NGS, EDTA Blood** Price
Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Niemann - Pick Disease Gene Panel by NGS, EDTA Blood** with a clear pricing structure.
The Niemann - Pick Disease Gene Panel by NGS, EDTA Blood** Price in Surat is ₹ 19,760 .
We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.
Frequently Asked Questions
This test measures various genes linked to Niemann-Pick disease. By identifying specific genetic mutations, healthcare providers can determine the risk of developing or passing on this genetic disorder. Understanding the genetic profile helps in providing appropriate treatment and genetic counselling for individuals and families affected by Niemann-Pick disease
- To diagnose Niemann-Pick disease accurately
- To assess the risk of inheriting or passing on this genetic disorder
- To guide the treatment plan for patients affected by Niemann-Pick disease
The Niemann-Pick Disease Gene Panel Test is recommended for:
- Individuals showing symptoms like enlarged liver or spleen, lung problems, or neurological issues
- Patients with a family history of Niemann-Pick disease
- Newborns with abnormal screening tests suggesting lipid storage disorders
Abnormal results indicate:
- Increased risk of developing or passing on Niemann-Pick disease
- Need for further confirmatory tests and consultations with a genetic counsellor or specialist
- A blood sample is usually collected for genetic analysis
- The procedure is quick and relatively painless
- A phlebotomist will draw blood from a vein in your arm using a needle
- The blood sample is then sent to a laboratory for genetic testing
- Follow any instructions given by your healthcare provider
- Inform your doctor about any medications, supplements, or health conditions you have
- DNA Sequencing: To identify specific mutations in genes related to Niemann-Pick disease
- Lysosomal Enzyme Assays: To assess enzyme deficiencies linked to lipid storage disorders
Genetic Analysis Panel for Niemann-Pick Disease or Gene Analysis Panel for Niemann-Pick Disease
Niemann-Pick disease is an inherited disorder characterized by lipid metabolism abnormalities, resulting in lipid accumulation in organs like the liver, spleen, brain, and lungs. The symptoms can differ significantly based on the specific type of Niemann-Pick disease and may include hepatosplenomegaly, lung problems, and neurological issues
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Why Metropolis?
Metropolis has a team of 200 senior pathologists and over 2000 technicians delivering diagnostic solutions in the areas of routine, semi specialty and super specialty domains like Oncology, Neurology, Gynaecology, Nephrology and many more.
We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.
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