STIM1 Gene Stormorken Syndrome Genetic Test sale cost 4400 AED
ADA2 Gene Sneddon Syndrome Genetic Test sale cost 4400 AED ADA2 Gene Sneddon Syndrome Genetic Test 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Genetic Mapping for Cardiovascular Disorders Test sale cost 4100 AED Genetic Mapping for Cardiovascular Disorders Test 4,550 د.إ Original price was: 4,550 د.إ.4,100 د.إCurrent price is: 4,100 د.إ.
Sale!

STIM1 Gene Stormorken Syndrome Genetic Test

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

-21%

The STIM1 gene plays a crucial role in the regulation of calcium levels within cells, which is vital for various cellular functions. Mutations in the STIM1 gene can lead to Stormorken syndrome, a rare genetic disorder characterized by a spectrum of symptoms including thrombocytopenia (a condition involving low platelet counts), asplenia (absence of the spleen), severe muscle weakness, short stature, and other anomalies.

To diagnose this complex condition, genetic testing of the STIM1 gene is essential. DNA Labs UAE offers a specialized genetic test for Stormorken syndrome, targeting the STIM1 gene to identify mutations that may cause the disorder. This test is crucial for accurate diagnosis, which can then guide appropriate treatment and management strategies for affected individuals.

The cost of the STIM1 gene test for Stormorken syndrome at DNA Labs UAE is 4400 AED. This investment covers the detailed analysis required to detect the genetic variations linked to the syndrome, providing essential information for patients and their families. Given the complexity of the condition and the tailored medical care needed by those affected, the test represents a critical step towards understanding and managing Stormorken syndrome.

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
Guaranteed Safe Checkout

STIM1 Gene Stormorken Syndrome 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: Vascular Diseases
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information:

Clinical History of Patient who is going for STIM1 Gene Stormorken Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with STIM1 Gene Stormorken Syndrome NGS Genetic DNA Test gene STIM1.

Test Details:

The STIM1 gene is associated with Stormorken syndrome, a rare genetic disorder characterized by a variety of symptoms including bleeding tendencies, muscle weakness, and short stature. NGS (Next-Generation Sequencing) is a type of genetic test that can be used to analyze multiple genes simultaneously. In the context of Stormorken syndrome, NGS can be used to sequence the STIM1 gene to identify any genetic variations or mutations that may be responsible for the disorder. This can help in confirming a diagnosis and providing genetic counseling for affected individuals and their families.

Test Name STIM1 Gene Stormorken syndrome 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 Vascular Diseases
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for STIM1 Gene Stormorken syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with STIM1 Gene Stormorken syndrome NGS Genetic DNA Test gene STIM1
Test Details

The STIM1 gene is associated with Stormorken syndrome, a rare genetic disorder characterized by a variety of symptoms including bleeding tendencies, muscle weakness, and short stature.

NGS (Next-Generation Sequencing) is a type of genetic test that can be used to analyze multiple genes simultaneously. In the context of Stormorken syndrome, NGS can be used to sequence the STIM1 gene to identify any genetic variations or mutations that may be responsible for the disorder. This can help in confirming a diagnosis and providing genetic counseling for affected individuals and their families.

SKU: TEST-3551 Category:

Related products