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SOX10 Gene Waardenburg Syndrome Type 4C Genetic Test Cost

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

-21%

The SOX10 Gene Waardenburg Syndrome Type 4C Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the SOX10 gene, which are linked to Waardenburg Syndrome Type 4C (WS4C). Waardenburg Syndrome is a group of genetic conditions characterized by varying degrees of hearing loss, changes in skin, hair, and eye pigmentation, and, in some cases, Hirschsprung disease. Type 4C specifically involves a combination of these symptoms along with issues in the development of the neural crest, which can affect the gastrointestinal system.

The SOX10 gene plays a crucial role in the development of neural crest cells, which contribute to the formation of melanocytes, structures in the ear, and the enteric nervous system. Mutations in this gene can disrupt these processes, leading to the symptoms observed in Waardenburg Syndrome Type 4C. Identifying mutations in the SOX10 gene through this genetic test can provide definitive diagnosis of WS4C, guide treatment options, and offer vital information for family planning.

The test is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services. The cost of the SOX10 Gene Waardenburg Syndrome Type 4C Genetic Test is 4400 AED. This test is essential for individuals with a family history of Waardenburg Syndrome or those exhibiting symptoms associated with WS4C, as it offers a clear genetic basis for the condition, thereby facilitating targeted interventions and management strategies.

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  • This test is not intended for medical diagnosis or treatment
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SOX10 Gene Waardenburg Syndrome Type 4C 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 4C NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SOX10 Gene Waardenburg syndrome type 4C NGS Genetic DNA Test gene SOX10.

Test Details

The SOX10 gene is associated with Waardenburg syndrome type 4C, which is a rare genetic disorder characterized by hearing loss, changes in skin and hair pigmentation, and abnormalities of the eyes. The NGS (Next Generation Sequencing) genetic test is a method used to analyze the DNA sequence of the SOX10 gene to identify any variations or mutations that may be responsible for the development of Waardenburg syndrome type 4C. This test can help in confirming a diagnosis, providing genetic counseling, and guiding treatment options for individuals suspected of having this syndrome.

Test Name SOX10 Gene Waardenburg syndrome type 4C 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 4C NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SOX10 Gene Waardenburg syndrome type 4C NGS Genetic DNA Test gene SOX10
Test Details

The SOX10 gene is associated with Waardenburg syndrome type 4C, which is a rare genetic disorder characterized by hearing loss, changes in skin and hair pigmentation, and abnormalities of the eyes. The NGS (Next Generation Sequencing) genetic test is a method used to analyze the DNA sequence of the SOX10 gene to identify any variations or mutations that may be responsible for the development of Waardenburg syndrome type 4C. This test can help in confirming a diagnosis, providing genetic counseling, and guiding treatment options for individuals suspected of having this syndrome.