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KDM6A Gene Kabuki Syndrome Type 2 Genetic Test Cost

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

-21%

The KDM6A Gene Kabuki Syndrome Type 2 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the KDM6A gene, which are associated with Kabuki Syndrome Type 2. Kabuki syndrome is a rare, congenital disorder characterized by distinctive facial features, growth delays, intellectual disability, and various organ malformations. The test involves analyzing the patient’s DNA to detect any abnormalities or mutations in the KDM6A gene that could indicate the presence of the syndrome. This genetic testing is crucial for early diagnosis, which can significantly aid in the management and treatment of the condition. The cost of the test is 4400 AED, making it an accessible option for those seeking comprehensive genetic analysis in the UAE. By opting for this test at DNA Labs UAE, patients and their families can gain valuable insights into their genetic health, leading to better-informed healthcare decisions.

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KDM6A Gene Kabuki Syndrome Type 2 Genetic Test

Test Name: KDM6A Gene Kabuki Syndrome Type 2 Genetic Test

Components: DNA Labs UAE

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 KDM6A Gene Kabuki Syndrome Type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KDM6A Gene Kabuki Syndrome Type 2 NGS Genetic DNA Test gene KDM6A

Test Details

The KDM6A gene is associated with Kabuki Syndrome Type 2, which is a rare genetic disorder characterized by developmental delay, intellectual disability, distinctive facial features, and various other physical abnormalities.

NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Kabuki Syndrome Type 2, NGS Genetic Test can be used to identify mutations or variations in the KDM6A gene that may be responsible for causing the disorder.

By analyzing the DNA sample of an individual suspected to have Kabuki Syndrome Type 2, the NGS Genetic Test can provide information about any mutations or variations in the KDM6A gene. This information can help in confirming a diagnosis, understanding the underlying genetic cause, and providing appropriate medical management and genetic counseling for the individual and their family.

Test Name KDM6A Gene Kabuki 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 KDM6A Gene Kabuki syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KDM6A Gene Kabuki syndrome type 2 NGS Genetic DNA Test gene KDM6A
Test Details

The KDM6A gene is associated with Kabuki syndrome type 2, which is a rare genetic disorder characterized by developmental delay, intellectual disability, distinctive facial features, and various other physical abnormalities.

NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Kabuki syndrome type 2, NGS Genetic Test can be used to identify mutations or variations in the KDM6A gene that may be responsible for causing the disorder.

By analyzing the DNA sample of an individual suspected to have Kabuki syndrome type 2, the NGS Genetic Test can provide information about any mutations or variations in the KDM6A gene. This information can help in confirming a diagnosis, understanding the underlying genetic cause, and providing appropriate medical management and genetic counseling for the individual and their family.