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PRKCD Gene Autoimmune Lymphoproliferative Syndrome Type 3 Genetic Test Cost

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

-21%

The PRKCD Gene Autoimmune Lymphoproliferative Syndrome Type 3 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the PRKCD gene, which are associated with Autoimmune Lymphoproliferative Syndrome Type 3 (ALPS Type 3). ALPS is a rare genetic disorder characterized by the abnormal proliferation of lymphocytes, leading to lymphadenopathy, splenomegaly, and an increased risk of autoimmune disorders and lymphomas. The PRKCD gene plays a crucial role in the programmed cell death pathway, and mutations in this gene can disrupt the balance of immune cell proliferation and apoptosis, contributing to the development of ALPS.

This test is crucial for individuals with clinical symptoms of ALPS or with a family history of the disorder, as it can provide a definitive diagnosis, guiding treatment options and management strategies. Conducted at the state-of-the-art facilities of DNA Labs UAE, the test ensures high accuracy and reliability. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to perform this sophisticated genetic analysis. Early diagnosis through the PRKCD Gene Autoimmune Lymphoproliferative Syndrome Type 3 Genetic Test can significantly improve the quality of life for affected individuals by enabling targeted therapies and close monitoring to prevent complications associated with the disease.

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PRKCD Gene Autoimmune Lymphoproliferative Syndrome Type 3 Genetic Test

Cost: AED 4400.0

Test Details

The PRKCD gene is associated with autoimmune lymphoproliferative syndrome type 3 (ALPS3). ALPS is a rare genetic disorder characterized by defective regulation of lymphocyte apoptosis, leading to the accumulation of lymphocytes in various organs and tissues.

NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of ALPS3, NGS genetic testing can be used to identify mutations or variants in the PRKCD gene that may be causing the disorder.

The test involves obtaining a DNA sample, usually through a blood sample, and sequencing the entire coding region of the PRKCD gene. This allows for the detection of small changes, such as single nucleotide variants (SNVs), insertions, deletions, or larger structural variants.

NGS genetic testing can provide valuable information for diagnosing ALPS3 and determining the specific genetic cause of the disorder. It can also be used for carrier testing and family planning purposes.

It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate counseling and guidance based on the test results.

Test Components

  • Price: AED 4400.0
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for PRKCD Gene Autoimmune lymphoproliferative syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRKCD Gene Autoimmune lymphoproliferative syndrome type 3 NGS Genetic DNA Test gene PRKCD.

Test Name PRKCD Gene Autoimmune lymphoproliferative syndrome type 3 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PRKCD Gene Autoimmune lymphoproliferative syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRKCD Gene Autoimmune lymphoproliferative syndrome type 3 NGS Genetic DNA Test gene PRKCD
Test Details

The PRKCD gene is associated with autoimmune lymphoproliferative syndrome type 3 (ALPS3). ALPS is a rare genetic disorder characterized by defective regulation of lymphocyte apoptosis, leading to the accumulation of lymphocytes in various organs and tissues.

NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. In the context of ALPS3, NGS genetic testing can be used to identify mutations or variants in the PRKCD gene that may be causing the disorder.

The test involves obtaining a DNA sample, usually through a blood sample, and sequencing the entire coding region of the PRKCD gene. This allows for the detection of small changes, such as single nucleotide variants (SNVs), insertions, deletions, or larger structural variants.

NGS genetic testing can provide valuable information for diagnosing ALPS3 and determining the specific genetic cause of the disorder. It can also be used for carrier testing and family planning purposes.

It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate counseling and guidance based on the test results.