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STAMBP Gene Microcephaly-Capillary Malformation Syndrome Genetic Test Cost

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

-21%

The STAMBP Gene Microcephaly-Capillary Malformation Syndrome Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the STAMBP gene, which are associated with Microcephaly-Capillary Malformation Syndrome (MIC-CAP). This rare genetic disorder is characterized by microcephaly, where an infant’s head is significantly smaller than expected, and capillary malformations, which are distinctive, small, red to purple spots on the skin. The condition may also involve a range of other physical and developmental challenges.

DNA Labs UAE provides this crucial genetic testing service for a fee of 4400 AED. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in their state-of-the-art laboratory. The aim is to detect any abnormalities in the STAMBP gene that could indicate the presence of MIC-CAP syndrome. This information is vital for early diagnosis, which can significantly impact the management and treatment of the condition, allowing healthcare providers to offer targeted support and interventions to improve the quality of life for affected individuals and their families.

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STAMBP Gene Microcephaly-capillary malformation syndrome Genetic Test

Genetic testing is an important tool in diagnosing and managing genetic disorders. One such test is the STAMBP Gene Microcephaly-capillary malformation syndrome Genetic Test offered by DNA Labs UAE.

Test Name: STAMBP Gene Microcephaly-capillary malformation syndrome Genetic Test

  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the STAMBP Gene Microcephaly-capillary malformation syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the syndrome. This information can help in the interpretation of the test results and provide valuable insights for managing the condition.

Test Details

The STAMBP gene is associated with microcephaly-capillary malformation syndrome (MIC-CAP), a rare genetic disorder characterized by abnormally small head size (microcephaly) and abnormalities in the small blood vessels (capillary malformations). The NGS genetic testing method used in this test allows for the simultaneous analysis of multiple genes.

By analyzing the STAMBP gene, this test can identify any mutations or variations that may be present, confirming a diagnosis of MIC-CAP. Additionally, it provides information about the specific genetic changes involved, which can be valuable for genetic counseling and managing the condition.

Test Name STAMBP Gene Microcephaly-capillary malformation syndrome Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for STAMBP Gene Microcephaly-capillary malformation syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with STAMBP Gene Microcephaly-capillary malformation syndrome
Test Details

The STAMBP gene is associated with microcephaly-capillary malformation syndrome (MIC-CAP) which is a rare genetic disorder characterized by microcephaly (abnormally small head size) and capillary malformations (abnormalities in the small blood vessels).

NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of microcephaly-capillary malformation syndrome, NGS genetic testing can be used to analyze the STAMBP gene to identify any mutations or variations that may be present. This can help in confirming a diagnosis of MIC-CAP and can also provide information about the specific genetic changes involved, which can be useful for genetic counseling and management of the condition.

SKU: TEST-1671 Category:

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