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PEX1 Gene Heimler Syndrome Type 1 Genetic Test Cost

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

-21%

The PEX1 Gene Heimler Syndrome Type 1 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the PEX1 gene, which are associated with Heimler Syndrome Type 1. Heimler Syndrome is a rare genetic disorder characterized by sensorineural hearing loss, dental anomalies, and, in some cases, visual impairments due to retinal dystrophy. The condition follows an autosomal recessive inheritance pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

This genetic test is crucial for the early diagnosis and management of Heimler Syndrome, allowing for timely intervention and support for affected individuals. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to identify any mutations in the PEX1 gene.

The cost of the PEX1 Gene Heimler Syndrome Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to accurately detect the presence of the genetic mutations associated with the syndrome. Early diagnosis through this test can significantly impact the quality of life for individuals with Heimler Syndrome, providing a pathway to appropriate treatments and support services.

Description

PEX1 Gene Heimler syndrome type 1 Genetic Test

Test Name: PEX1 Gene Heimler syndrome type 1 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: Ear Nose Throat Disorders

Doctor: ENT Doctor

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA14

Test Details: PEX1 gene Heimler syndrome type 1 NGS genetic test is a type of genetic test that is used to detect mutations in the PEX1 gene. Heimler syndrome type 1 is a rare genetic disorder characterized by sensorineural hearing loss, intellectual disability, and various physical abnormalities. NGS stands for next-generation sequencing, which is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of this genetic test, NGS is used to sequence the PEX1 gene and identify any mutations or variations that may be present. This test can be useful in confirming a diagnosis of Heimler syndrome type 1 and providing information about the specific genetic cause of the disorder. It can also be used for carrier testing in individuals with a family history of Heimler syndrome type 1. The results of the test can help guide treatment and management decisions, as well as provide information about the risk of passing the condition on to future generations. It is important to note that genetic testing should be done in conjunction with clinical evaluation and counseling by a healthcare professional experienced in genetics.

Test Name	PEX1 Gene Heimler syndrome type 1 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 EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EYA1 Gene Branchiootic syndrome type 1 NGS Genetic DNA Test gene EYA14
Test Details	PEX1 gene Heimler syndrome type 1 NGS genetic test is a type of genetic test that is used to detect mutations in the PEX1 gene. Heimler syndrome type 1 is a rare genetic disorder characterized by sensorineural hearing loss, intellectual disability, and various physical abnormalities. NGS stands for next-generation sequencing, which is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of this genetic test, NGS is used to sequence the PEX1 gene and identify any mutations or variations that may be present. This test can be useful in confirming a diagnosis of Heimler syndrome type 1 and providing information about the specific genetic cause of the disorder. It can also be used for carrier testing in individuals with a family history of Heimler syndrome type 1. The results of the test can help guide treatment and management decisions, as well as provide information about the risk of passing the condition on to future generations. It is important to note that genetic testing should be done in conjunction with clinical evaluation and counseling by a healthcare professional experienced in genetics.