RTTN Gene Microcephaly Short Stature and Polymicrogyria with Seizures Genetic Test
At DNA Labs UAE, we offer the RTTN Gene Microcephaly Short Stature and Polymicrogyria with Seizures Genetic Test to help diagnose and understand this genetic condition. This test can provide valuable information for genetic counseling, family planning, and potential treatment options.
Test Details
The RTTN gene is associated with a genetic condition called microcephaly, short stature, and polymicrogyria with seizures. This condition is characterized by a small head size (microcephaly), short stature, and abnormal brain development (polymicrogyria) leading to seizures.
To diagnose this condition, we perform a Next-Generation Sequencing (NGS) genetic test. NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes or the entire genome. It can detect variations or mutations in the RTTN gene that may be responsible for the observed symptoms.
Test Components and Price
The cost of the RTTN Gene Microcephaly Short Stature and Polymicrogyria with Seizures Genetic Test is 4400.0 AED. The test involves analyzing the DNA sample using NGS technology.
Sample Condition
We accept blood samples, extracted DNA, or one drop of blood on an FTA card for this test.
Report Delivery
You can expect to receive the test results within 3 to 4 weeks after sample submission.
Test Type
The RTTN Gene Microcephaly Short Stature and Polymicrogyria with Seizures Genetic Test falls under the category of dysmorphology.
Doctor and Test Department
This test is performed under the supervision of a pediatrician in our Genetics department.
Pre Test Information
Before undergoing the RTTN Gene Microcephaly Short Stature and Polymicrogyria with Seizures 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 this genetic condition.
Genetic counseling can help in understanding the inheritance pattern and assessing the risk of passing on the condition to future generations.
Conclusion
The RTTN Gene Microcephaly Short Stature and Polymicrogyria with Seizures Genetic Test offered by DNA Labs UAE can provide valuable insights into this genetic condition. By identifying variations or mutations in the RTTN gene, we can confirm the diagnosis and provide important information for genetic counseling, family planning, and potential treatment options.
Test Name | RTTN Gene Microcephaly short stature and polymicrogyria with seizures Genetic Test |
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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 RTTN Gene Microcephaly, short stature, and polymicrogyria with seizures NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RTTN Gene Microcephaly, short stature, and polymicrogyria with seizures NGS Genetic DNA Test gene RTTN |
Test Details |
The RTTN gene is associated with a genetic condition called microcephaly, short stature, and polymicrogyria with seizures. This condition is characterized by a small head size (microcephaly), short stature, and abnormal brain development (polymicrogyria) leading to seizures. To diagnose this condition, a Next-Generation Sequencing (NGS) genetic test can be performed. NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes or the entire genome. It can detect variations or mutations in the RTTN gene that may be responsible for the observed symptoms. The NGS genetic test involves collecting a DNA sample, typically through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology, and the resulting data is analyzed for variations in the RTTN gene. If a mutation or variation is identified in the RTTN gene, it can confirm the diagnosis of microcephaly, short stature, and polymicrogyria with seizures. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options. |