TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test
Test Name: TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test
Components: TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test
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 TMCO1 Gene Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TMCO1 Gene Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome
Test Details: The TMCO1 gene is associated with a rare genetic disorder known as Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome. This syndrome is characterized by a range of physical and developmental abnormalities, including distinctive facial features, skeletal abnormalities, intellectual disability, and delayed development of motor skills. NGS genetic testing can be used to identify mutations in the TMCO1 gene that may be responsible for this syndrome. This type of testing involves sequencing the entire coding region of the gene to identify any changes or mutations that may be present. Identification of TMCO1 gene mutations can provide valuable information for families affected by this syndrome, including information about inheritance patterns, recurrence risks, and potential treatment options. It can also help clinicians better understand the underlying mechanisms of the disorder and develop more targeted therapies in the future.
| Test Name | TMCO1 Gene Craniofacial dysmorphism skeletal anomalies and mental retardation syndrome 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 TMCO1 Gene Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TMCO1 Gene Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome |
| Test Details |
The TMCO1 gene is associated with a rare genetic disorder known as Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome. This syndrome is characterized by a range of physical and developmental abnormalities, including distinctive facial features, skeletal abnormalities, intellectual disability, and delayed development of motor skills. NGS genetic testing can be used to identify mutations in the TMCO1 gene that may be responsible for this syndrome. This type of testing involves sequencing the entire coding region of the gene to identify any changes or mutations that may be present. Identification of TMCO1 gene mutations can provide valuable information for families affected by this syndrome, including information about inheritance patterns, recurrence risks, and potential treatment options. It can also help clinicians better understand the underlying mechanisms of the disorder and develop more targeted therapies in the future. |
