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PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 Genetic Test Cost

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

-21%

The PGAP2 gene is associated with Hyperphosphatasia with Mental Retardation Syndrome Type 3 (HPMRS3), a rare genetic disorder characterized by significantly elevated levels of alkaline phosphatase, intellectual disability, and various physical anomalies. The PGAP2 gene plays a crucial role in the modification of proteins that are essential for normal brain development and function. Mutations in the PGAP2 gene disrupt these processes, leading to the symptoms observed in HPMRS3.

To diagnose this condition, a genetic test focusing on the PGAP2 gene can be conducted. This test is crucial for confirming the diagnosis, understanding the disease’s progression, and facilitating the management of symptoms. It involves analyzing the DNA for mutations in the PGAP2 gene that are known to cause HPMRS3.

In the United Arab Emirates, DNA Labs UAE offers this specific genetic test for HPMRS3. The cost of the test is 4400 AED. Conducting the test at DNA Labs UAE ensures accuracy and reliability, as the lab is equipped with advanced genetic testing technologies and staffed by experts in the field. This test is a valuable resource for families seeking answers about HPMRS3, providing them with crucial information for making informed decisions about care and management.

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PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 Genetic Test

Test Name: PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PGAP2 Gene Hyperphosphatasia with Mental Retardation Syndrome Type 3 NGS Genetic DNA Test gene PGAP2

Test Details: PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3 is a rare genetic disorder characterized by intellectual disability and elevated levels of alkaline phosphatase in the blood. It is caused by mutations in the PGAP2 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3, NGS genetic testing can be used to identify mutations in the PGAP2 gene that are responsible for the disorder. NGS genetic testing involves extracting DNA from a patient’s blood or saliva sample and then sequencing the DNA to identify any genetic variations or mutations. This can help in diagnosing the specific genetic cause of the disorder and providing information for genetic counseling and management of the condition. It is important to consult with a healthcare professional or genetic counselor to discuss the benefits, limitations, and implications of NGS genetic testing for PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3. They can provide guidance on the appropriateness of the test, potential risks, and available support services.

Test Name PGAP2 Gene Hyperphosphatasia with mental retardation 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PGAP2 Gene Hyperphosphatasia with mental retardation syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PGAP2 Gene Hyperphosphatasia with mental retardation syndrome type 3 NGS Genetic DNA Test gene PGAP2
Test Details

PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3 is a rare genetic disorder characterized by intellectual disability and elevated levels of alkaline phosphatase in the blood. It is caused by mutations in the PGAP2 gene.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3, NGS genetic testing can be used to identify mutations in the PGAP2 gene that are responsible for the disorder.

NGS genetic testing involves extracting DNA from a patient’s blood or saliva sample and then sequencing the DNA to identify any genetic variations or mutations. This can help in diagnosing the specific genetic cause of the disorder and providing information for genetic counseling and management of the condition.

It is important to consult with a healthcare professional or genetic counselor to discuss the benefits, limitations, and implications of NGS genetic testing for PGAP2 gene hyperphosphatasia with mental retardation syndrome type 3. They can provide guidance on the appropriateness of the test, potential risks, and available support services.

SKU: TEST-4168 Category:

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