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Myotonic Dystrophy Comprehensive Profile Test Cost

Original price was: 2,080 د.إ.Current price is: 1,870 د.إ.

-10%

The Myotonic Dystrophy Comprehensive Profile Test is a specialized diagnostic evaluation offered by DNA Labs UAE, designed to identify the genetic markers associated with Myotonic Dystrophy, a form of muscular dystrophy that affects muscle function and other body systems. This test plays a critical role in diagnosing the condition, enabling healthcare providers to tailor treatment plans and offer genetic counseling based on the results. Priced at 1870 AED, the test involves analyzing specific DNA sequences to detect mutations in the DMPK gene for Myotonic Dystrophy Type 1 or the CNBP gene for Type 2, which are the primary genetic contributors to the disorder. Conducted in the advanced facilities of DNA Labs UAE, this comprehensive profile provides valuable insights for patients and their families, guiding management and care decisions for those affected by Myotonic Dystrophy.

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MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE Test

Test Name: MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE Test

Test Components: DMPK Gene, ZFN9 Gene

Price: 1870.0 AED

Sample Condition: 4 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.

Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Report Delivery: SampleMon by 11 am; Report Fri

Method: PCR, Fragment Analysis

Test Type: Neurologic Disorder

Doctor: Neurologist

Test Department: MOLECULAR DIAGNOSTICS

Pre Test Information: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Test Details

The MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE test is a diagnostic tool used to assess and diagnose myotonic dystrophy, a genetic disorder that affects the muscles and other body systems. This test analyzes specific genetic markers associated with myotonic dystrophy to determine if an individual has the condition.

The test typically involves a blood or saliva sample, which is sent to a laboratory for analysis. The laboratory will examine the sample for the presence of certain genetic mutations, such as expansions of the CTG repeat in the DMPK gene for type 1 myotonic dystrophy or the CCTG repeat in the ZNF9 gene for type 2 myotonic dystrophy.

In addition to identifying the specific genetic mutation, the MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE test may also provide information about the severity and progression of the condition. This can help healthcare providers develop a personalized treatment plan and provide appropriate care and support to individuals with myotonic dystrophy.

It is important to note that the MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE test is a specialized test and is typically ordered by a healthcare provider who suspects myotonic dystrophy based on an individual’s symptoms and family history. The test results should be interpreted by a qualified healthcare professional who can provide appropriate counseling and guidance based on the findings.

Test Name MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE Test
Components *DMPK Gene*ZFN9 Gene
Price 1870.0 AED
Sample Condition 4 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery SampleMon by 11 am; Report Fri
Method PCR, Fragment Analysis
Test type Neurologic Disorder
Doctor Neurologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

The MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE test is a diagnostic tool used to assess and diagnose myotonic dystrophy, a genetic disorder that affects the muscles and other body systems. This test analyzes specific genetic markers associated with myotonic dystrophy to determine if an individual has the condition.

The test typically involves a blood or saliva sample, which is sent to a laboratory for analysis. The laboratory will examine the sample for the presence of certain genetic mutations, such as expansions of the CTG repeat in the DMPK gene for type 1 myotonic dystrophy or the CCTG repeat in the ZNF9 gene for type 2 myotonic dystrophy.

In addition to identifying the specific genetic mutation, the MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE test may also provide information about the severity and progression of the condition. This can help healthcare providers develop a personalized treatment plan and provide appropriate care and support to individuals with myotonic dystrophy.

It is important to note that the MYOTONIC DYSTROPHY COMPREHENSIVE PROFILE test is a specialized test and is typically ordered by a healthcare provider who suspects myotonic dystrophy based on an individual’s symptoms and family history. The test results should be interpreted by a qualified healthcare professional who can provide appropriate counseling and guidance based on the findings.