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PIGT Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 Genetic Test Cost

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

-21%

The PIGT Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 (MCAHS3) genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the PIGT gene, which can lead to the development of MCAHS3. This syndrome is a rare genetic disorder characterized by a spectrum of symptoms including multiple congenital anomalies, muscle hypotonia (reduced muscle tone), and seizures, among others. The genetic test plays a crucial role in the early diagnosis and management of the syndrome, allowing for timely intervention and support for affected individuals.

The test is conducted through a detailed analysis of the patient’s DNA to detect abnormalities in the PIGT gene that are indicative of MCAHS3. This is crucial for understanding the specific genetic alterations in an individual, which can help in tailoring personalized treatment and management plans. The cost of the test is set at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the PIGT gene.

By opting for this genetic test at DNA Labs UAE, patients and their families can gain valuable insights into the genetic underpinnings of the syndrome, facilitating informed decisions regarding care and management. It is an important step towards improving the quality of life for individuals with MCAHS3 through targeted interventions and support.

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PIGT Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 Genetic Test

At DNA Labs UAE, we offer the PIGT Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 Genetic Test. This test is designed to identify mutations or variations in the PIGT gene that may be responsible for the syndrome.

Test Details

The PIGT gene is associated with a rare genetic disorder called Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 (MCAHS3). This syndrome is characterized by developmental delay, intellectual disability, seizures, hypotonia, facial dysmorphism, and various congenital anomalies.

The PIGT Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 Genetic Test is performed using Next-Generation Sequencing (NGS) technology. NGS is a high-throughput sequencing method that allows for the analysis of multiple genes simultaneously.

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

Prior to undergoing the PIGT Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the syndrome.

Genetic counseling and management of the condition can be facilitated by the information obtained from NGS genetic testing. This test can also help identify carriers of the gene mutation within a family, allowing for early detection and intervention in at-risk individuals.

For more information or to schedule an appointment, please contact our Genetics Test Department.

Test Name PIGT Gene Multiple congenital anomalies-hypotonia-seizures syndrome type 3 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 PIGT Gene Multiple congenital anomalies-hypotonia-seizures syndrome type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PIGT Gene Multiple congenital anomalies-hypotonia-seizures syndrome type 3
Test Details

The PIGT gene is associated with a rare genetic disorder called Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 (MCAHS3). This syndrome is characterized by a variety of symptoms including developmental delay, intellectual disability, seizures, hypotonia (low muscle tone), facial dysmorphism (abnormal facial features), and various congenital anomalies (birth defects).

NGS Genetic Test refers to Next-Generation Sequencing, which is a high-throughput sequencing technology used to analyze multiple genes simultaneously. In the context of MCAHS3, NGS genetic testing can be used to identify mutations or variations in the PIGT gene that may be responsible for the syndrome.

By analyzing the DNA sequence of the PIGT gene, NGS genetic testing can help confirm a diagnosis of MCAHS3 and provide valuable information for genetic counseling and management of the condition. It can also help identify carriers of the gene mutation within a family, allowing for early detection and intervention in at-risk individuals.

SKU: TEST-1738