SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Encephalomyopathic Type with Methylmalonic Aciduria Genetic Test
Are you looking for a genetic test to diagnose Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria? DNA Labs UAE offers the SUCLG1 Gene Mitochondrial DNA depletion syndrome encephalomyopathic type with methylmalonic aciduria Genetic Test at a cost of AED 4400.0.
Test Details
The SUCLG1 gene is associated with a rare genetic disorder called Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria. This disorder is characterized by a deficiency of the SUCLG1 enzyme, which is involved in the breakdown of certain molecules for energy production in the mitochondria.
NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the SUCLG1 gene and identify any mutations or variants that may be present. This test can help diagnose individuals with Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria by confirming the presence of mutations in the SUCLG1 gene.
Genetic testing can also provide information about the specific mutation(s) present, which can be helpful for determining the prognosis, inheritance pattern, and potential treatment options for affected individuals and their families. Additionally, genetic testing may be used for carrier testing and prenatal diagnosis in families with a known history of this disorder.
It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential risks associated with genetic testing before undergoing any testing procedures.
Test Components and Price
Test Name: SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Encephalomyopathic Type with Methylmalonic Aciduria Genetic Test
Components: NGS Technology
Price: 4400.0 AED
Sample Condition
Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery
3 to 4 Weeks
Test Type
Neurological Disorders
Doctor
Neurologist
Test Department
Genetics
Pre Test Information
Clinical History of Patient who is going for SUCLG1 Gene Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with SUCLG1 Gene Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria
Test Name | SUCLG1 Gene Mitochondrial DNA depletion syndrome encephalomyopathic type with methylmalonic aciduria 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 SUCLG1 Gene Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SUCLG1 Gene Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria |
Test Details |
The SUCLG1 gene is associated with a rare genetic disorder called Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria. This disorder is characterized by a deficiency of the SUCLG1 enzyme, which is involved in the breakdown of certain molecules for energy production in the mitochondria. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the SUCLG1 gene and identify any mutations or variants that may be present. This test can help diagnose individuals with Mitochondrial DNA depletion syndrome, encephalomyopathic type with methylmalonic aciduria by confirming the presence of mutations in the SUCLG1 gene. Genetic testing can also provide information about the specific mutation(s) present, which can be helpful for determining the prognosis, inheritance pattern, and potential treatment options for affected individuals and their families. Additionally, genetic testing may be used for carrier testing and prenatal diagnosis in families with a known history of this disorder. It is important to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential risks associated with genetic testing before undergoing any testing procedures. |