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SOX10 Gene Waardenburg Syndrome Type 2E Genetic Test Cost

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

-21%

The SOX10 Gene Waardenburg Syndrome Type 2E Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the SOX10 gene, which are linked to Waardenburg Syndrome Type 2E. This condition is a rare genetic disorder characterized by varying degrees of hearing loss, changes in skin pigmentation, and anomalies in hair and eye color. The SOX10 gene plays a critical role in the development of neural crest cells, which contribute to the formation of melanocytes, the cells responsible for pigment in the skin, hair, and eyes. Mutations in this gene can disrupt the normal development of these cells, leading to the symptoms associated with Waardenburg Syndrome Type 2E.

The test is priced at 4400 AED and involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any genetic alterations in the SOX10 gene. This genetic test is crucial for early diagnosis and management of the syndrome, allowing for timely interventions and support for affected individuals. It is also valuable for families seeking to understand their genetic makeup, especially if there is a history of Waardenburg Syndrome, providing them with essential information for family planning and genetic counseling. DNA Labs UAE, with its state-of-the-art facilities and expert team, ensures accurate and reliable testing services for those seeking insights into their genetic health.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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SOX10 Gene Waardenburg syndrome type 2E Genetic Test

Cost: 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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information:

Clinical History of Patient who is going for SOX10 Gene Waardenburg syndrome type 2E NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SOX10 Gene Waardenburg syndrome type 2E NGS Genetic DNA Test gene SOX10.

Test Details:

The SOX10 gene is associated with Waardenburg syndrome type 2E, a rare genetic disorder characterized by hearing loss, changes in pigmentation of the hair, skin, and eyes, and abnormalities of the eyes. NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously.

In the context of Waardenburg syndrome type 2E, an NGS genetic test can be performed to detect mutations or variations in the SOX10 gene, which can help in diagnosing the condition. During the test, a sample of DNA (usually obtained from blood or saliva) is analyzed to identify any changes in the SOX10 gene that may be responsible for the development of Waardenburg syndrome type 2E. The NGS technology allows for a comprehensive analysis of the gene, enabling the detection of both small and large genetic alterations.

The results of the NGS genetic test can provide valuable information for genetic counseling, family planning, and management of individuals with Waardenburg syndrome type 2E. It can help confirm the diagnosis, determine the inheritance pattern, and guide the appropriate medical interventions and support for affected individuals and their families.

Test Name SOX10 Gene Waardenburg syndrome type 2E 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SOX10 Gene Waardenburg syndrome type 2E NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SOX10 Gene Waardenburg syndrome type 2E NGS Genetic DNA Test gene SOX10
Test Details

The SOX10 gene is associated with Waardenburg syndrome type 2E, a rare genetic disorder characterized by hearing loss, changes in pigmentation of the hair, skin, and eyes, and abnormalities of the eyes.

NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Waardenburg syndrome type 2E, an NGS genetic test can be performed to detect mutations or variations in the SOX10 gene, which can help in diagnosing the condition.

During the test, a sample of DNA (usually obtained from blood or saliva) is analyzed to identify any changes in the SOX10 gene that may be responsible for the development of Waardenburg syndrome type 2E. The NGS technology allows for a comprehensive analysis of the gene, enabling the detection of both small and large genetic alterations.

The results of the NGS genetic test can provide valuable information for genetic counseling, family planning, and management of individuals with Waardenburg syndrome type 2E. It can help confirm the diagnosis, determine the inheritance pattern, and guide the appropriate medical interventions and support for affected individuals and their families.

SKU: TEST-3296 Category:

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