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KMT2C Gene Developmental Delay KMT2C Related Genetic Test

4,400 د.إ

-21%

The KMT2C gene is crucial in human development, playing a significant role in the regulation of gene expression through its involvement in chromatin modification. Mutations in the KMT2C gene can lead to a range of developmental delays and neurodevelopmental disorders, making it a key focus for genetic testing in individuals presenting with such clinical features.

At DNA Labs UAE, a specialized genetic test targeting the KMT2C gene is offered to diagnose conditions related to its mutations. This test is particularly important for families and individuals seeking a deeper understanding of developmental delays and seeking targeted interventions or therapies. 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 KMT2C gene that could be responsible for the observed clinical symptoms.

The cost of the KMT2C-related genetic test at DNA Labs UAE is set at 4400 AED. This price reflects the comprehensive nature of the test, encompassing the advanced genetic sequencing technologies used and the expert analysis required to interpret the results accurately. Given the potential impact of a KMT2C gene mutation on an individual’s development, this test represents a crucial step towards personalized medical care, offering insights that can guide therapeutic decisions and support.

It’s important for individuals considering this test to consult with a genetic counselor or a healthcare professional who can provide detailed information about the implications of the test results and the next steps in the management or treatment of conditions associated with KMT2C gene mutations.

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KMT2C Gene Developmental Delay – Genetic Testing at DNA Labs UAE

Are you concerned about developmental delay and related neurological disorders in your family? DNA Labs UAE offers the KMT2C Gene Developmental Delay Genetic Test to provide you with valuable insights into this condition.

Test Name: KMT2C Gene Developmental Delay

Test Components:

  • NGS Technology – Next-Generation Sequencing

Test 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:

Neurological Disorders

Referring Doctor:

Neurologist

Test Department:

Genetics

Pre-Test Information:

Before undergoing the KMT2C Gene Developmental Delay Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by KMT2C Gene Developmental Delay.

About the KMT2C Gene

The KMT2C gene, also known as MLL3, plays a crucial role in the regulation of gene expression during development. Mutations in this gene have been linked to developmental delay, intellectual disability, and various neurological and developmental disorders.

NGS Genetic Testing for KMT2C Gene

NGS (next-generation sequencing) genetic testing is used to identify mutations in the KMT2C gene and other genes associated with developmental delay. This advanced testing method allows for the sequencing of large amounts of DNA in a short period of time, enabling the detection of rare and complex genetic variations.

Implications and Recommendations

If a mutation is identified in the KMT2C gene, genetic counseling and further testing may be recommended for family members. This will help determine their risk of passing on the mutation to future generations.

Treatment and Management

The treatment and management of developmental delay and related conditions typically involve a multidisciplinary approach. This may include therapy, medication, and supportive care.

At DNA Labs UAE, we are committed to providing accurate and comprehensive genetic testing services. Our KMT2C Gene Developmental Delay Genetic Test can provide valuable information for individuals and families affected by this condition.

Test Name KMT2C Gene Developmental delay KMT2C related Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for KMT2C Gene Developmental delay, KMT2C related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with KMT2C Gene Developmental delay, KMT2C related
Test Details

The KMT2C gene, also known as MLL3, is involved in the regulation of gene expression during development. Mutations in this gene have been associated with developmental delay, intellectual disability, and other neurological and developmental disorders.

NGS (next-generation sequencing) genetic testing can be used to detect mutations in the KMT2C gene and other genes associated with developmental delay. This type of testing involves sequencing large amounts of DNA in a short amount of time, allowing for the identification of rare and complex genetic variations.

If a mutation is identified in the KMT2C gene, genetic counseling and further testing may be recommended for family members to determine their risk of passing on the mutation to future generations. Treatment and management of developmental delay and related conditions typically involve a multidisciplinary approach, including therapy, medication, and supportive care.