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KMT2A Gene Wiedemann-Steiner Syndrome Genetic Test Cost

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

-21%

The KMT2A Gene Wiedemann-Steiner Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the KMT2A gene, which are associated with Wiedemann-Steiner Syndrome (WSS). WSS is a rare genetic disorder characterized by distinctive facial features, developmental delay, short stature, and hypertrichosis. The test is crucial for the accurate diagnosis of the syndrome, enabling tailored treatment and management plans for affected individuals.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient’s DNA to detect any abnormalities in the KMT2A gene. The cost of the test is 4400 AED, reflecting the comprehensive analysis and the sophisticated technology employed to ensure accurate results. By opting for this test, patients and their families can gain valuable insights into the genetic underpinnings of WSS, facilitating informed decisions regarding care and support.

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KMT2A Gene Wiedemann-Steiner syndrome Genetic Test

At DNA Labs UAE, we offer the KMT2A Gene Wiedemann-Steiner syndrome Genetic Test at a cost of AED 4400.0.

Test Components

Price: AED 4400.0

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 KMT2A Gene Wiedemann-Steiner syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KMT2A Gene Wiedemann-Steiner syndrome NGS Genetic DNA Test gene KMT2A.

Test Details

The KMT2A gene, also known as the MLL gene, is associated with a genetic disorder called Wiedemann-Steiner syndrome. This syndrome is characterized by developmental delay, intellectual disability, hypertrichosis (excessive hair growth), distinctive facial features, and short stature.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that analyzes multiple genes simultaneously to identify variations or mutations in the DNA sequence. This type of testing can be used to diagnose genetic disorders like Wiedemann-Steiner syndrome by identifying specific mutations or variations in the KMT2A gene.

NGS genetic testing for Wiedemann-Steiner syndrome typically involves obtaining a DNA sample, usually through a blood or saliva sample, and sequencing the DNA to identify any variations or mutations in the KMT2A gene.

The results of the test can help confirm a diagnosis of Wiedemann-Steiner syndrome and guide appropriate medical management and treatment options.

It is important to consult with a genetic counselor or healthcare provider to discuss the appropriateness and availability of NGS genetic testing for Wiedemann-Steiner syndrome. They can provide more information about the specific testing process, potential risks and benefits, and implications of the test results.

Test Name KMT2A Gene Wiedemann-Steiner syndrome 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 KMT2A Gene Wiedemann-Steiner syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KMT2A Gene Wiedemann-Steiner syndrome NGS Genetic DNA Test gene KMT2A
Test Details

The KMT2A gene, also known as the MLL gene, is associated with a genetic disorder called Wiedemann-Steiner syndrome. This syndrome is characterized by developmental delay, intellectual disability, hypertrichosis (excessive hair growth), distinctive facial features, and short stature.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that analyzes multiple genes simultaneously to identify variations or mutations in the DNA sequence. This type of testing can be used to diagnose genetic disorders like Wiedemann-Steiner syndrome by identifying specific mutations or variations in the KMT2A gene.

NGS genetic testing for Wiedemann-Steiner syndrome typically involves obtaining a DNA sample, usually through a blood or saliva sample, and sequencing the DNA to identify any variations or mutations in the KMT2A gene. The results of the test can help confirm a diagnosis of Wiedemann-Steiner syndrome and guide appropriate medical management and treatment options.

It is important to consult with a genetic counselor or healthcare provider to discuss the appropriateness and availability of NGS genetic testing for Wiedemann-Steiner syndrome. They can provide more information about the specific testing process, potential risks and benefits, and implications of the test results.

SKU: TEST-4441 Category:

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