ZMPSTE24 Gene Mandibuloacral Dysplasia with Type B Lipodystrophy Genetic Test
Are you or a loved one experiencing symptoms of mandibuloacral dysplasia with type B lipodystrophy? The ZMPSTE24 Gene Mandibuloacral Dysplasia with Type B Lipodystrophy Genetic Test offered by DNA Labs UAE may provide the answers you need. In this blog, we will discuss the test components, cost, symptoms, diagnosis, and other important details.
Test Name: ZMPSTE24 Gene Mandibuloacral Dysplasia with Type B Lipodystrophy Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Osteology Dermatology Immunology Disorders
Doctor: Dermatologist
Test Department: Genetics
Pre Test Information: It is important to provide the clinical history of the patient who is going for the ZMPSTE24 Gene Mandibuloacral Dysplasia with Type B Lipodystrophy NGS Genetic DNA Test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with the gene ZMPSTE24.
Test Details
The ZMPSTE24 Gene Mandibuloacral Dysplasia with Type B Lipodystrophy NGS genetic test is a diagnostic test that utilizes next-generation sequencing (NGS) technology to analyze the ZMPSTE24 gene for mutations associated with mandibuloacral dysplasia with type B lipodystrophy.
Mandibuloacral dysplasia with type B lipodystrophy is a rare genetic disorder characterized by skeletal abnormalities, lipodystrophy (loss of body fat), and other features such as joint stiffness, skin changes, and heart problems. This condition is caused by mutations in the ZMPSTE24 gene, which plays a role in the processing of a protein called prelamin A.
NGS genetic testing allows for the simultaneous analysis of multiple genes, including the ZMPSTE24 gene, in a more efficient and cost-effective manner compared to traditional Sanger sequencing. This test can identify different types of mutations in the ZMPSTE24 gene, such as point mutations, insertions, deletions, and duplications.
The results of the NGS genetic test can help confirm a diagnosis of mandibuloacral dysplasia with type B lipodystrophy and guide appropriate medical management and genetic counseling for affected individuals and their families. It is important to note that this test is typically performed in specialized genetic testing laboratories and requires a healthcare provider’s order.
If you suspect that you or a family member may have mandibuloacral dysplasia with type B lipodystrophy, it is crucial to consult with a dermatologist or other healthcare professional who can provide the necessary guidance and order the ZMPSTE24 Gene Mandibuloacral Dysplasia with Type B Lipodystrophy Genetic Test.
At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to learn more about the ZMPSTE24 Gene Mandibuloacral Dysplasia with Type B Lipodystrophy Genetic Test and how it can help in the diagnosis and management of this rare genetic disorder.
Test Name | ZMPSTE24 Gene Mandibuloacral dysplasia with type B lipodystrophy 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 ZMPSTE24 Gene Mandibuloacral dysplasia with type B lipodystrophy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZMPSTE24 Gene Mandibuloacral dysplasia with type B lipodystrophy NGS Genetic DNA Test gene ZMPSTE24 |
Test Details |
ZMPSTE24 gene mandibuloacral dysplasia with type B lipodystrophy NGS genetic test is a diagnostic test that uses next-generation sequencing (NGS) technology to analyze the ZMPSTE24 gene for mutations associated with mandibuloacral dysplasia with type B lipodystrophy. Mandibuloacral dysplasia with type B lipodystrophy is a rare genetic disorder characterized by skeletal abnormalities, lipodystrophy (loss of body fat), and other features such as joint stiffness, skin changes, and heart problems. It is caused by mutations in the ZMPSTE24 gene, which is involved in the processing of a protein called prelamin A. NGS genetic testing allows for the simultaneous analysis of multiple genes, including the ZMPSTE24 gene, in a more efficient and cost-effective manner compared to traditional Sanger sequencing. This test can identify different types of mutations in the ZMPSTE24 gene, including point mutations, insertions, deletions, and duplications. The results of the NGS genetic test can help confirm a diagnosis of mandibuloacral dysplasia with type B lipodystrophy and guide appropriate medical management and genetic counseling for affected individuals and their families. It is important to note that this test is typically performed in specialized genetic testing laboratories and requires a healthcare provider’s order. |