NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 Genetic Test sale cost 4400 AED
TMEM70 Gene Mitochondrial Complex V ATP Synthase Deficiency Nuclear Type 2 Genetic Test sale cost 4400 AED TMEM70 Gene Mitochondrial Complex V ATP Synthase Deficiency Nuclear Type 2 Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
PABPN1 Gene Muscular Dystrophy Oculopharyngeal Genetic Test sale cost 4400 AED PABPN1 Gene Muscular Dystrophy Oculopharyngeal Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 Genetic Test Cost

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

-21%

The NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE. Priced at 4400 AED, this test is designed to identify mutations in the NFU1 gene, which are associated with Multiple Mitochondrial Dysfunctions Syndrome Type 1 (MMDS1). MMDS1 is a rare genetic disorder characterized by a wide range of symptoms, including developmental delay, neurological deterioration, and metabolic abnormalities, stemming from impaired mitochondrial function.

Mitochondria are known as the powerhouses of the cell, and their dysfunction can lead to severe and often life-threatening conditions. The NFU1 gene plays a crucial role in the biosynthesis of iron-sulfur (Fe-S) clusters, essential components for mitochondrial energy production. Mutations in the NFU1 gene disrupt this process, leading to the symptoms observed in MMDS1.

The test conducted at DNA Labs UAE involves collecting a DNA sample, typically through a blood draw, and analyzing it for specific mutations in the NFU1 gene. This genetic test is critical for early diagnosis, which can significantly influence the management and treatment strategies for affected individuals. Early intervention may include dietary modifications, supplements, and supportive therapies aimed at improving quality of life and mitigating the progression of symptoms.

In summary, the NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 Genetic Test is a valuable diagnostic tool for identifying the genetic cause of MMDS1, facilitating early and effective management of the disorder. Offered at DNA Labs UAE for 4400 AED, this test represents a crucial step towards personalized care for individuals with this rare mitochondrial condition.

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

NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 Genetic Test

Are you or your loved ones experiencing symptoms related to NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1? DNA Labs UAE offers a comprehensive genetic test to diagnose this rare genetic disorder. Read on to find out more about the test, its components, cost, and other important details.

Test Name

NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to the NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by this syndrome.

Test Details

NFU1 gene multiple mitochondrial dysfunctions syndrome type 1 is a rare genetic disorder characterized by multiple mitochondrial dysfunctions. It is caused by mutations in the NFU1 gene, responsible for producing a protein involved in the assembly of iron-sulfur clusters in mitochondria.

NGS genetic testing, also known as next-generation sequencing, is a type of genetic test that uses advanced sequencing technology to rapidly analyze multiple genes or the entire genome. In the context of NFU1 gene multiple mitochondrial dysfunctions syndrome type 1, NGS genetic testing can be used to identify mutations in the NFU1 gene.

The test involves obtaining a DNA sample, usually through a blood sample or cheek swab, and sequencing the DNA to identify any variations or mutations in the NFU1 gene. This information can help confirm a diagnosis of NFU1 gene multiple mitochondrial dysfunctions syndrome type 1 and guide treatment and management options.

NGS genetic testing is a powerful tool in the field of genetic medicine as it can analyze large amounts of genetic data quickly and accurately. It provides valuable information for diagnosing genetic disorders, identifying disease-causing mutations, and guiding personalized treatment plans.

If you suspect NFU1 gene multiple mitochondrial dysfunctions syndrome type 1 or have any questions regarding the genetic test, we recommend consulting with a neurologist. DNA Labs UAE is dedicated to providing accurate and reliable genetic testing services to help individuals and families understand their genetic health.

Test Name NFU1 Gene Multiple mitochondrial dysfunctions syndrome type 1 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 NFU1 Gene Multiple mitochondrial dysfunctions syndrome type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NFU1 Gene Multiple mitochondrial dysfunctions syndrome type 1
Test Details

NFU1 gene multiple mitochondrial dysfunctions syndrome type 1 is a rare genetic disorder characterized by multiple mitochondrial dysfunctions. It is caused by mutations in the NFU1 gene, which is responsible for producing a protein involved in the assembly of iron-sulfur clusters in mitochondria.

NGS genetic testing, also known as next-generation sequencing, is a type of genetic test that uses advanced sequencing technology to rapidly analyze multiple genes or the entire genome. In the context of NFU1 gene multiple mitochondrial dysfunctions syndrome type 1, NGS genetic testing can be used to identify mutations in the NFU1 gene.

The test involves obtaining a DNA sample, usually through a blood sample or cheek swab, and sequencing the DNA to identify any variations or mutations in the NFU1 gene. This information can help confirm a diagnosis of NFU1 gene multiple mitochondrial dysfunctions syndrome type 1 and guide treatment and management options.

NGS genetic testing is a powerful tool in the field of genetic medicine, as it can analyze large amounts of genetic data quickly and accurately. It can provide valuable information for diagnosing genetic disorders, identifying disease-causing mutations, and guiding personalized treatment plans.

SKU: TEST-1739 Category:

Related products