IER3IP1 Gene Microcephaly with Epilepsy and Diabetes Syndrome Genetic Test sale cost 4400 AED
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IER3IP1 Gene Microcephaly with Epilepsy and Diabetes Syndrome Genetic Test Cost

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

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The IER3IP1 Gene Microcephaly with Epilepsy and Diabetes Syndrome Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at identifying mutations in the IER3IP1 gene. These mutations are known to be associated with a rare, inherited disorder characterized by microcephaly (a condition where a baby’s head is significantly smaller than expected), epilepsy, and diabetes syndrome. This comprehensive test is crucial for families seeking answers to developmental delays, seizures, and other related symptoms in their children, providing them with vital information for management and treatment plans.

The test, priced at 4400 AED, involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the state-of-the-art facilities at DNA Labs UAE. The laboratory employs advanced genetic sequencing technologies to accurately identify any mutations in the IER3IP1 gene, ensuring reliable results. By opting for this test, families can gain insights into the genetic underpinnings of the condition, enabling healthcare providers to tailor interventions and support to meet the specific needs of the affected individual.

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IER3IP1 Gene Microcephaly with epilepsy and diabetes syndrome Genetic Test

Test Cost: AED 4400.0

Symptoms and Diagnosis

Microcephaly with epilepsy and diabetes syndrome is a rare genetic disorder characterized by microcephaly (abnormally small head size), epilepsy (seizures), and diabetes. To diagnose this syndrome, a genetic test for the IER3IP1 gene is conducted.

Test Components and Details

The IER3IP1 Gene Microcephaly with epilepsy and diabetes syndrome Genetic Test is performed using NGS (Next-Generation Sequencing) technology. This method allows for the analysis of an individual’s DNA sequence to identify genetic mutations or variants in the IER3IP1 gene.

Sample Condition:

The sample required for the test can be either blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery:

The test results are typically delivered within 3 to 4 weeks.

Test Type:

The test falls under the category of Dysmorphology.

Doctor:

The test is recommended for Pediatrics patients.

Test Department:

The test is conducted in the Genetics department.

Pre Test Information

Prior to undergoing the IER3IP1 Gene Microcephaly with epilepsy and diabetes syndrome NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by this genetic disorder.

Test Process

The test involves collecting a sample of the individual’s DNA, usually through a blood sample or a cheek swab. The collected DNA is then subjected to NGS sequencing, which allows for the detection of specific genetic variants or mutations in the IER3IP1 gene.

Importance of Test Results

If a mutation or variant is identified in the IER3IP1 gene through NGS testing, it can provide valuable information for diagnosing Microcephaly with epilepsy and diabetes syndrome. This information can guide medical management and treatment options for individuals affected by this rare genetic disorder.

Test Name IER3IP1 Gene Microcephaly with epilepsy and diabetes 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for IER3IP1 Gene Microcephaly with epilepsy and diabetes syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IER3IP1 Gene Microcephaly with epilepsy and diabetes syndrome NGS Genetic DNA Test gene IER3IP1
Test Details

The IER3IP1 gene is associated with a rare genetic disorder called Microcephaly with epilepsy and diabetes syndrome. This syndrome is characterized by microcephaly (abnormally small head size), epilepsy (seizures), and diabetes.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual. It can be used to identify genetic mutations or variants in specific genes, such as the IER3IP1 gene. By analyzing the DNA sequence, NGS testing can help diagnose genetic disorders, including Microcephaly with epilepsy and diabetes syndrome.

The NGS genetic test for IER3IP1 gene mutations involves collecting a sample of the individual’s DNA, usually through a blood sample or a cheek swab. The DNA is then sequenced using advanced technology, which allows for the detection of specific genetic variants or mutations in the IER3IP1 gene.

If a mutation or variant is identified in the IER3IP1 gene through NGS testing, it can provide valuable information for diagnosing Microcephaly with epilepsy and diabetes syndrome. This can help guide medical management and treatment options for individuals with this rare genetic disorder.

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