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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 assessment offered by DNA Labs UAE, designed to identify mutations in the PLCB4 gene, which are linked to Auriculocondylar syndrome type 2 (ACS2). This condition is a rare genetic disorder characterized by craniofacial abnormalities, such as malformations of the ears and mandible (lower jaw). The test plays a crucial role in the accurate diagnosis and understanding of ACS2, facilitating targeted management and genetic counseling for affected families.

The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic variations in the PLCB4 gene that are associated with the syndrome. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and detailed report provided by DNA Labs UAE. By offering this test, DNA Labs UAE supports healthcare professionals and families in identifying and addressing Auriculocondylar syndrome type 2, contributing to improved patient outcomes and quality of life.

Description

PLCB4 Gene Auriculocondylar Syndrome Type 2 Genetic Test

Test Name: PLCB4 Gene Auriculocondylar Syndrome Type 2 Genetic Test

Components: PLCB4 Gene Auriculocondylar Syndrome 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: Ear Nose Throat Disorders

Doctor: ENT Doctor

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 a rare genetic disorder called Auriculocondylar Syndrome Type 2 (ARCND2). This syndrome affects the development of the ears, jaw, and other facial features. NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of variations or mutations in the DNA sequence that may be responsible for genetic disorders like ARCND2.

The PLCB4 Gene Auriculocondylar Syndrome Type 2 NGS Genetic Test specifically focuses on sequencing the PLCB4 gene to identify any variations or mutations that may be present. This test can help diagnose individuals with ARCND2 and provide information about the specific genetic cause of their condition.

Genetic testing for ARCND2 can be beneficial for individuals with symptoms suggestive of the disorder, as it can confirm the diagnosis and provide important information for medical management and genetic counseling. It can also be used for carrier testing in families with a known history of ARCND2 to determine the risk of passing the condition on to future generations.

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	Ear Nose Throat Disorders
Doctor	ENT Doctor
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 a rare genetic disorder called Auriculocondylar syndrome type 2 (ARCND2). This syndrome affects the development of the ears, jaw, and other facial features. NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of variations or mutations in the DNA sequence that may be responsible for genetic disorders like ARCND2. The PLCB4 Gene Auriculocondylar syndrome type 2 NGS Genetic Test specifically focuses on sequencing the PLCB4 gene to identify any variations or mutations that may be present. This test can help diagnose individuals with ARCND2 and provide information about the specific genetic cause of their condition. Genetic testing for ARCND2 can be beneficial for individuals with symptoms suggestive of the disorder, as it can confirm the diagnosis and provide important information for medical management and genetic counseling. It can also be used for carrier testing in families with a known history of ARCND2 to determine the risk of passing the condition on to future generations.