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SLC39A13 Gene Spondylocheirodysplasia Ehlers-Danlos Syndrome-Like Genetic Test Cost

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

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The SLC39A13 gene is associated with a rare genetic condition known as Spondylocheirodysplasia, Ehlers-Danlos Syndrome-like (SCD-EDS). This condition is characterized by a combination of skeletal and connective tissue abnormalities, including but not limited to, short stature, hyperelastic skin, and distinctive facial features. The SLC39A13 gene plays a crucial role in the regulation of zinc transport in cells, which is essential for the normal development and maintenance of connective tissue.

To diagnose this condition, a specific genetic test can be performed, which involves analyzing the SLC39A13 gene for mutations that are known to cause Spondylocheirodysplasia, Ehlers-Danlos Syndrome-like. This test is crucial for confirming the diagnosis, understanding the inheritance pattern, and providing appropriate genetic counseling to affected families.

In the UAE, DNA Labs offers this genetic testing service. The test cost is 4400 AED. DNA Labs UAE is a reputable institution known for its advanced genetic testing capabilities, providing accurate and reliable results. Opting for this test at DNA Labs UAE ensures that individuals and families receive comprehensive support, from the initial consultation to the interpretation of results and guidance on the subsequent steps.

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SLC39A13 Gene Spondylocheirodysplasia Ehlers-Danlos syndrome-like Genetic Test

Are you or a loved one experiencing symptoms of Spondylocheirodysplasia Ehlers-Danlos syndrome-like (SCD-EDS)? DNA Labs UAE offers a comprehensive genetic test to help diagnose this rare genetic disorder.

Test Details

The SLC39A13 gene is associated with SCD-EDS, a condition characterized by skeletal abnormalities, joint hypermobility, and skin findings similar to Ehlers-Danlos syndrome. Our Next-Generation Sequencing (NGS) genetic test utilizes advanced sequencing technology to analyze multiple genes simultaneously.

By identifying mutations or variants in the SLC39A13 gene, our test can provide a definitive diagnosis for individuals suspected of having SCD-EDS. This information is crucial for guiding medical management and understanding the inheritance pattern of the condition.

Test Components and Price

Our SLC39A13 Gene Spondylocheirodysplasia Ehlers-Danlos syndrome-like Genetic Test is priced at 4400.0 AED.

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Reports are typically delivered within 3 to 4 weeks.

Test Type

This test falls under the categories of Osteology, Dermatology, and Immunology Disorders.

Doctor and Test Department

Our genetic test is performed by our experienced dermatologists in our Genetics department.

Pre Test Information

Prior to the test, we recommend providing the clinical history of the patient who is going for the SLC39A13 Gene Spondylocheirodysplasia Ehlers-Danlos syndrome-like NGS Genetic DNA Test. A genetic counseling session will also be conducted to draw a pedigree chart of family members affected by SCD-EDS.

Genetic Counseling

Genetic testing for SCD-EDS should be ordered and interpreted by a healthcare professional with expertise in genetics. We strongly recommend genetic counseling before and after testing to discuss the implications of the results and provide support for individuals and families.

Don’t wait any longer to get answers. Contact DNA Labs UAE today to schedule your SLC39A13 Gene Spondylocheirodysplasia Ehlers-Danlos syndrome-like Genetic Test and take the first step towards a definitive diagnosis.

Test Name SLC39A13 Gene Spondylocheirodysplasia Ehlers-Danlos syndrome-like 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 SLC39A13 Gene Spondylocheirodysplasia, Ehlers-Danlos syndrome-like NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC39A13 Gene Spondylocheirodysplasia, Ehlers-Danlos syndrome-like NGS Genetic DNA Test gene SLC39A13
Test Details

The SLC39A13 gene is associated with a rare genetic disorder called Spondylocheirodysplasia Ehlers-Danlos syndrome-like (SCD-EDS). This condition is characterized by a combination of skeletal abnormalities, joint hypermobility, and skin findings similar to Ehlers-Danlos syndrome.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of SCD-EDS, NGS genetic testing can be used to identify mutations or variants in the SLC39A13 gene that are associated with this condition.

The purpose of this genetic test is to provide a definitive diagnosis for individuals suspected of having SCD-EDS. It can help confirm the presence of specific mutations in the SLC39A13 gene, which can guide medical management and provide information about the inheritance pattern of the condition.

It’s important to note that genetic testing for SCD-EDS should be ordered and interpreted by a healthcare professional with expertise in genetics. Genetic counseling is also recommended before and after testing to discuss the implications of the results and provide support for individuals and families.

SKU: TEST-3259 Category:

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