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DMPK Gene Myotonic Dystrophy Type 1 Genetic Test Cost

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

-21%

The DMPK Gene Myotonic Dystrophy Type 1 Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the DMPK gene, which are responsible for causing Myotonic Dystrophy Type 1 (DM1). This condition is characterized by progressive muscle loss and weakness, myotonia, and various other systemic issues. The test involves analyzing the patient’s DNA to identify the specific genetic alteration within the DMPK gene, known as a CTG triplet repeat expansion. The presence and size of the expansion can help in confirming the diagnosis of DM1 and predicting the severity of the condition.

Offered by DNA Labs UAE, this genetic test is a critical tool for individuals suspected of having Myotonic Dystrophy Type 1 or for those with a family history of the disease, aiming to provide a clear genetic diagnosis. The test is priced at 4400 AED and is conducted in a state-of-the-art laboratory setting, ensuring high accuracy and reliability of the results. Through this test, patients and their families can gain valuable insights into the genetic basis of the condition, which can significantly aid in managing the disease and planning for the future.

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DMPK Gene Myotonic Dystrophy Type 1 Genetic Test

Test Name: DMPK Gene Myotonic dystrophy type 1 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 DMPK Gene Myotonic dystrophy type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DMPK Gene Myotonic dystrophy type 1.

About DMPK Gene Myotonic Dystrophy Type 1

The DMPK gene is associated with myotonic dystrophy type 1 (DM1), a genetic disorder characterized by progressive muscle wasting and weakness. NGS (next-generation sequencing) genetic testing is a technique used to analyze the DNA sequence of genes, including the DMPK gene, to identify any genetic mutations or variations that may be associated with DM1.

NGS genetic testing for DM1 can provide information about the size of the CTG repeat expansion in the DMPK gene, which is the primary genetic abnormality in this disorder. The number of CTG repeats in the gene is directly correlated with the severity and age of onset of DM1 symptoms. A higher number of CTG repeats typically leads to an earlier onset and more severe symptoms.

NGS testing can also identify other genetic variations in the DMPK gene that may contribute to the development or progression of DM1. This information can be used for diagnostic purposes, as well as for genetic counseling and family planning.

Overall, NGS genetic testing for the DMPK gene in DM1 can help in the diagnosis, prognosis, and management of individuals with this condition. It can also provide important information for family members who may be at risk of inheriting the disease.

For more information or to schedule a DMPK Gene Myotonic Dystrophy Type 1 Genetic Test, please contact DNA Labs UAE.

Test Name DMPK Gene Myotonic dystrophy 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 DMPK Gene Myotonic dystrophy type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DMPK Gene Myotonic dystrophy type 1
Test Details

The DMPK gene is associated with myotonic dystrophy type 1 (DM1), which is a genetic disorder characterized by progressive muscle wasting and weakness. NGS (next-generation sequencing) genetic testing is a technique used to analyze the DNA sequence of genes, including the DMPK gene, to identify any genetic mutations or variations that may be associated with DM1.

NGS genetic testing for DM1 can provide information about the size of the CTG repeat expansion in the DMPK gene, which is the primary genetic abnormality in this disorder. The number of CTG repeats in the gene is directly correlated with the severity and age of onset of DM1 symptoms. A higher number of CTG repeats typically leads to an earlier onset and more severe symptoms.

NGS testing can also identify other genetic variations in the DMPK gene that may contribute to the development or progression of DM1. This information can be used for diagnostic purposes, as well as for genetic counseling and family planning.

Overall, NGS genetic testing for the DMPK gene in DM1 can help in the diagnosis, prognosis, and management of individuals with this condition. It can also provide important information for family members who may be at risk of inheriting the disease.

SKU: TEST-1815 Category:

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