RELN Gene Lissencephaly type 2 Norman-Roberts type Genetic Test
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 RELN Gene Lissencephaly type 2 (Norman-Roberts type) NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RELN Gene Lissencephaly type 2 (Norman-Roberts type) NGS Genetic DNA Test gene RELN
Test Details
Gene Lissencephaly type 2, also known as Norman-Roberts type, is a rare genetic disorder characterized by smooth brain (lissencephaly) and severe intellectual disability. It is caused by mutations in the RELN gene.
NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Gene Lissencephaly type 2, NGS Genetic Test can be used to identify mutations in the RELN gene that are associated with this disorder.
The NGS Genetic Test involves obtaining a DNA sample from the patient, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology, which allows for the detection of small genetic variations or mutations in the RELN gene.
By identifying the specific mutations in the RELN gene, the NGS Genetic Test can provide a definitive diagnosis of Gene Lissencephaly type 2. This information can be helpful in understanding the underlying cause of the disorder, predicting its progression, and potentially guiding treatment options.
It is important to note that genetic testing, including NGS Genetic Test, should be performed under the guidance of a healthcare professional or genetic counselor. They can help interpret the results, provide appropriate genetic counseling, and discuss the implications of the diagnosis.
| Test Name | RELN Gene Lissencephaly type 2 Norman-Roberts type 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 RELN Gene Lissencephaly type 2 (Norman-Roberts type) NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RELN Gene Lissencephaly type 2 (Norman-Roberts type) NGS Genetic DNA Test gene RELN |
| Test Details |
Gene Lissencephaly type 2, also known as Norman-Roberts type, is a rare genetic disorder characterized by smooth brain (lissencephaly) and severe intellectual disability. It is caused by mutations in the RELN gene. NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Gene Lissencephaly type 2, NGS Genetic Test can be used to identify mutations in the RELN gene that are associated with this disorder. The NGS Genetic Test involves obtaining a DNA sample from the patient, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology, which allows for the detection of small genetic variations or mutations in the RELN gene. By identifying the specific mutations in the RELN gene, the NGS Genetic Test can provide a definitive diagnosis of Gene Lissencephaly type 2. This information can be helpful in understanding the underlying cause of the disorder, predicting its progression, and potentially guiding treatment options. It is important to note that genetic testing, including NGS Genetic Test, should be performed under the guidance of a healthcare professional or genetic counselor. They can help interpret the results, provide appropriate genetic counseling, and discuss the implications of the diagnosis. |
