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. |
