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TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test Cost

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

-21%

The TPP1 gene test for Ceroid Lipofuscinosis Neuronal Type 2 (CLN2), also known as late infantile Batten disease, is a crucial genetic screening conducted at DNA Labs UAE. This test, priced at 4400 AED, is designed to identify mutations in the TPP1 gene, which are responsible for CLN2. The condition is a rare, inherited, neurodegenerative disorder characterized by the accumulation of lipopigments in the body’s tissues, leading to symptoms such as seizures, dementia, visual loss, and motor dysfunction. Early diagnosis through the TPP1 gene test is vital for managing symptoms and potentially accessing enzyme replacement therapies that can slow disease progression. DNA Labs UAE employs state-of-the-art genetic testing technologies to ensure accurate and reliable results for patients and their families seeking insights into this genetic condition.

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TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test

Welcome to DNA Labs UAE, where we offer the TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test. This test is designed to identify any genetic variants or mutations in the TPP1 gene that may be responsible for ceroid lipofuscinosis neuronal type 2 (CLN2), a rare genetic disorder characterized by the accumulation of lipopigments in the cells of the central nervous system.

Test Details

The TPP1 gene is associated with ceroid lipofuscinosis neuronal type 2 (CLN2). Our Next-Generation Sequencing (NGS) technology allows us to analyze the DNA sequence of the TPP1 gene to identify any genetic variants or mutations that may be present. This information can help in the diagnosis of CLN2 and may also be used for carrier testing or prenatal testing in families with a known history of the condition.

Components

  • Test Name: TPP1 Gene Ceroid lipofuscinosis neuronal type 2 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

Prior to the TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with Ceroid lipofuscinosis neuronal type 2. This information will help in the interpretation of the test results and provide a comprehensive understanding of the genetic condition.

Cost

The cost of the TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test is 4400.0 AED.

Symptoms and Diagnosis

Ceroid lipofuscinosis neuronal type 2 (CLN2) is characterized by the accumulation of lipopigments in the cells of the central nervous system. Symptoms may include progressive loss of motor skills, seizures, vision loss, and cognitive decline. Diagnosis of CLN2 is typically made through genetic testing, such as the TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test, along with clinical evaluation and medical history.

Conclusion

The TPP1 Gene Ceroid lipofuscinosis neuronal type 2 Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing and understanding ceroid lipofuscinosis neuronal type 2 (CLN2). With our advanced NGS technology and expert team of geneticists, we are committed to providing accurate and reliable results to help patients and their families in managing this rare genetic disorder.

Test Name TPP1 Gene Ceroid lipofuscinosis neuronal type 2 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 TPP1 Gene Ceroid lipofuscinosis neuronal type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Ceroid lipofuscinosis neuronal type 2
Test Details

The TPP1 gene is associated with ceroid lipofuscinosis neuronal type 2 (CLN2), which is a rare genetic disorder characterized by the accumulation of lipopigments in the cells of the central nervous system. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of the TPP1 gene to identify any genetic variants or mutations that may be responsible for CLN2. This type of genetic testing can help in the diagnosis of CLN2 and may also be used for carrier testing or prenatal testing in families with a known history of the condition.

SKU: TEST-2208 Category:

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