ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test
Introduction to the ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test
The ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test is a specialized diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to identify genetic mutations associated with KBG syndrome. This condition, characterized by developmental delays, distinctive facial features, and skeletal abnormalities, can significantly impact the quality of life for affected individuals and their families. Understanding the genetic basis of KBG syndrome is crucial for timely intervention and management.
What the Test Measures
This genetic test specifically measures alterations in the ANKRD11 gene, which is known to play a role in various developmental processes. By analyzing the DNA, the test can detect specific mutations that are linked to the manifestation of KBG syndrome.
Who Should Consider This Test?
Individuals who may benefit from the ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test include:
- Children exhibiting developmental delays or learning difficulties.
- Individuals with characteristic facial features associated with KBG syndrome.
- Families with a history of genetic disorders or symptoms suggestive of KBG syndrome.
Benefits of Taking the Test
Taking the ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test offers numerous benefits:
- Accurate diagnosis of KBG syndrome, enabling tailored treatment plans.
- Providing families with information regarding the inheritance patterns of the condition.
- Facilitating genetic counseling and support for affected families.
Understanding Your Results
Results from the ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test will typically be available within 3 to 4 weeks. A genetic counselor will assist in interpreting the results, helping families understand the implications of any identified mutations, and guiding them through the next steps in management.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 NGN |
Regular Price | 560,000 NGN |
Book the Test
To book the ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test or for more information, please contact us at +2348110567037. Our team is ready to assist you and provide the necessary support for your health needs.
Pre-Test Instructions
Before undergoing the ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test, it is essential to have a clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected by KBG syndrome.
Specialty and Department
This test falls under the specialty of Pediatrics and the department of Genetics, utilizing NGS Technology to diagnose the disease type known as Dysmorphology.