WDR62 Gene Microcephaly with Cortical Malformations Autosomal Recessive Type 2 Genetic Test
Test Name: WDR62 Gene Microcephaly with cortical malformations autosomal recessive type 2 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 WDR62 Gene Microcephaly with cortical malformations, autosomal recessive type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WDR62 Gene Microcephaly with cortical malformations, autosomal recessive type 2 NGS Genetic DNA Test gene WDR62
Test Details: The WDR62 gene is associated with a condition called microcephaly with cortical malformations, autosomal recessive type 2. This condition is characterized by small head size (microcephaly) and abnormalities in the development of the cerebral cortex, which is the outer layer of the brain responsible for higher cognitive functions. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes. It can identify variations or mutations in specific genes, including the WDR62 gene, that may be responsible for a particular condition or disease. In the context of microcephaly with cortical malformations, autosomal recessive type 2, NGS genetic testing can help confirm a diagnosis by identifying mutations in the WDR62 gene. This information can be important for understanding the underlying cause of the condition and for providing appropriate medical management and genetic counseling for affected individuals and their families. It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate recommendations.
| Test Name | WDR62 Gene Microcephaly with cortical malformations autosomal recessive type 2 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 WDR62 Gene Microcephaly with cortical malformations, autosomal recessive type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WDR62 Gene Microcephaly with cortical malformations, autosomal recessive type 2 NGS Genetic DNA Test gene WDR62 |
| Test Details | The WDR62 gene is associated with a condition called microcephaly with cortical malformations, autosomal recessive type 2. This condition is characterized by small head size (microcephaly) and abnormalities in the development of the cerebral cortex, which is the outer layer of the brain responsible for higher cognitive functions. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes. It can identify variations or mutations in specific genes, including the WDR62 gene, that may be responsible for a particular condition or disease. In the context of microcephaly with cortical malformations, autosomal recessive type 2, NGS genetic testing can help confirm a diagnosis by identifying mutations in the WDR62 gene. This information can be important for understanding the underlying cause of the condition and for providing appropriate medical management and genetic counseling for affected individuals and their families. It’s important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate recommendations. |
