Sale!

SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Encephalomyopathic Type with Methylmalonic Aciduria Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Encephalomyopathic Type with Methylmalonic Aciduria Genetic Test is a specialized diagnostic assessment offered at DNA Labs UAE. This test is specifically designed to identify mutations in the SUCLG1 gene, which are known to cause a rare, inherited condition characterized by mitochondrial DNA depletion syndrome (MDS). The encephalomyopathic type of this syndrome is particularly severe, leading to neurological impairment, muscle weakness, and a range of other systemic symptoms. Additionally, affected individuals often exhibit methylmalonic aciduria, an abnormal accumulation of methylmalonic acid in the blood, which can lead to metabolic complications.

The test is conducted through a comprehensive analysis of the patient’s DNA to detect any mutations in the SUCLG1 gene that are indicative of this condition. Early diagnosis through genetic testing is crucial for managing symptoms, preventing complications, and providing targeted treatments to improve the quality of life for affected individuals.

The cost of the SUCLG1 Gene Mitochondrial DNA Depletion Syndrome Encephalomyopathic Type with Methylmalonic Aciduria Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the detailed and specialized process of genetic analysis required to accurately diagnose this complex condition, enabling healthcare providers to devise an effective treatment plan tailored to the genetic profile of the patient.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

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.