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PLCB4 Gene Auriculocondylar Syndrome Type 2 Genetic Test Cost

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

-21%

The PLCB4 Gene Auriculocondylar Syndrome Type 2 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the PLCB4 gene, which are linked to Auriculocondylar Syndrome Type 2 (ACS2). ACS2 is a rare genetic disorder characterized by anomalies in the structure of the ear (auricular) and the mandible (condylar), among other possible symptoms including facial asymmetry and issues with the heart and lungs. This condition is inherited in an autosomal dominant pattern, meaning a single copy of the altered gene in each cell is sufficient to cause the disorder.

The test, priced at 4400 AED, involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed to detect mutations in the PLCB4 gene. Early diagnosis through genetic testing like the PLCB4 Gene Auriculocondylar Syndrome Type 2 Genetic Test is crucial for the management of the condition. It enables healthcare providers to offer appropriate treatments and interventions, and allows families to understand the risk of passing the condition to future generations. Conducted in the advanced facilities of DNA Labs UAE, this test represents a key step in the journey towards personalized medicine for patients with ACS2, offering them hope for a better quality of life through tailored care and management strategies.

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PLCB4 Gene Auriculocondylar syndrome type 2 Genetic Test

At DNA Labs UAE, we offer the PLCB4 Gene Auriculocondylar syndrome type 2 Genetic Test. This test is designed to identify mutations or variations in the PLCB4 gene that may be responsible for Auriculocondylar syndrome type 2, a rare genetic disorder characterized by abnormalities of the ears, mandible (lower jaw), and other facial structures.

Test Details

The PLCB4 Gene Auriculocondylar syndrome type 2 Genetic Test is performed using NGS (Next-Generation Sequencing) technology. NGS genetic testing allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the case of Auriculocondylar syndrome type 2, this test can help confirm a diagnosis by detecting variations in the PLCB4 gene.

Test Components and Price

  • Test Name: PLCB4 Gene Auriculocondylar syndrome type 2 Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the PLCB4 Gene Auriculocondylar syndrome type 2 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 disorder. This will help in the interpretation of the test results and provide valuable information for genetic counseling and management of the condition.

How the Test Works

To perform the PLCB4 Gene Auriculocondylar syndrome type 2 Genetic Test, a DNA sample is required. This can be obtained through a blood sample or cheek swab. The DNA is then sequenced using high-throughput sequencing technology, allowing for the detection of variations in multiple genes simultaneously. The results of the test can confirm a diagnosis of Auriculocondylar syndrome type 2 and provide important information for further medical guidance.

Please note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor who specializes in genetics. They can provide appropriate counseling and guidance based on the test results.

Test Name PLCB4 Gene Auriculocondylar syndrome 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PLCB4 Gene Auriculocondylar syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PLCB4 Gene Auriculocondylar syndrome type 2 NGS Genetic DNA Test gene PLCB4
Test Details

The PLCB4 gene is associated with Auriculocondylar syndrome type 2, which is a rare genetic disorder characterized by abnormalities of the ears, mandible (lower jaw), and other facial structures.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the case of Auriculocondylar syndrome type 2, NGS genetic testing can be used to identify mutations or variations in the PLCB4 gene that may be responsible for the disorder.

NGS genetic testing typically involves obtaining a DNA sample, usually through a blood sample or cheek swab. The DNA is then sequenced using high-throughput sequencing technology, allowing for the detection of variations in multiple genes simultaneously. The results of the test can help confirm a diagnosis of Auriculocondylar syndrome type 2 and provide valuable information for genetic counseling and management of the condition.

It’s important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who specializes in genetics. They can provide appropriate counseling and guidance based on the test results.

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