NEXMIF Gene Mental Retardation X-linked Nonsyndromic Genetic Test
Test Name: NEXMIF Gene Mental Retardation X-linked Nonsyndromic Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for NEXMIF Gene Mental Retardation, X-linked, nonsyndromic NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NEXMIF Gene Mental Retardation, X-linked, nonsyndromic.
Test Details
The NEXMIF gene is associated with a condition called mental retardation, X-linked, nonsyndromic (MRX). MRX is a type of intellectual disability that primarily affects males. It is characterized by significant limitations in intellectual functioning and adaptive behavior.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of MRX, NGS genetic testing can be used to identify mutations or variants in the NEXMIF gene that may be responsible for the condition.
NGS genetic testing involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual undergoing testing. The DNA is then sequenced using advanced technologies to analyze the entire coding region of the NEXMIF gene. The obtained sequencing data is compared to a reference genome to identify any genetic variations or mutations.
By identifying mutations or variants in the NEXMIF gene, NGS genetic testing can provide a genetic diagnosis for individuals with MRX. This information can be useful for understanding the underlying cause of the condition, predicting the risk of recurrence in future pregnancies, and guiding treatment and management strategies.
It is important to note that NGS genetic testing may not identify a causative mutation in all cases, as the genetic basis of MRX can be complex and involve other genes as well. Additionally, genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics.
| Test Name | NEXMIF Gene Mental retardation X-linked nonsyndromic 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 NEXMIF Gene Mental retardation, X-linked, nonsyndromic NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NEXMIF Gene Mental retardation, X-linked, nonsyndromic |
| Test Details |
The NEXMIF gene is associated with a condition called mental retardation, X-linked, nonsyndromic (MRX). MRX is a type of intellectual disability that primarily affects males. It is characterized by significant limitations in intellectual functioning and adaptive behavior. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of MRX, NGS genetic testing can be used to identify mutations or variants in the NEXMIF gene that may be responsible for the condition. NGS genetic testing involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual undergoing testing. The DNA is then sequenced using advanced technologies to analyze the entire coding region of the NEXMIF gene. The obtained sequencing data is compared to a reference genome to identify any genetic variations or mutations. By identifying mutations or variants in the NEXMIF gene, NGS genetic testing can provide a genetic diagnosis for individuals with MRX. This information can be useful for understanding the underlying cause of the condition, predicting the risk of recurrence in future pregnancies, and guiding treatment and management strategies. It is important to note that NGS genetic testing may not identify a causative mutation in all cases, as the genetic basis of MRX can be complex and involve other genes as well. Additionally, genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics. |
