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DYM Gene Dyggve-Melchior-Clausen disease Genetic Test Cost

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

-21%

The DYM gene Dyggve-Melchior-Clausen (DMC) disease genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the DYM gene, which are responsible for Dyggve-Melchior-Clausen disease. This rare genetic disorder is characterized by skeletal abnormalities, short trunk dwarfism, and, in some cases, developmental delays. The test plays a crucial role in the early detection and management of the condition, enabling healthcare providers to devise appropriate treatment and intervention strategies. Conducted in a state-of-the-art facility, the test ensures accuracy and reliability in results. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the advanced technology employed in the testing process.

Description

DYM Gene Dyggve-Melchior-Clausen Disease Genetic Test

Test Name: DYM Gene Dyggve-Melchior-Clausen Disease 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

Method: Next Generation Sequencing (NGS) Technology

Test Type: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for DYM Gene Dyggve-Melchior-Clausen Disease NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Dyggve-Melchior-Clausen Disease.

Test Details: DYM Gene Dyggve-Melchior-Clausen Disease NGS Genetic Test is a genetic test that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the DYM gene. This gene is associated with Dyggve-Melchior-Clausen Disease, which is a rare genetic disorder characterized by skeletal abnormalities and intellectual disability.

The NGS Genetic Test analyzes the DNA of an individual to identify any mutations or variations in the DYM gene that may be responsible for causing the disease. This test can help in confirming a diagnosis of Dyggve-Melchior-Clausen Disease and also provide information about the specific mutation present in an individual.

The test is usually performed on a blood or saliva sample and involves sequencing the DNA to detect any variations in the DYM gene. The results of the test can help in determining the genetic cause of the disease, predicting the prognosis, and guiding appropriate treatment and management strategies.

It is important to note that this test is typically performed in specialized genetic testing laboratories and requires a referral from a healthcare provider or genetic counselor. The test results should be interpreted by a healthcare professional with expertise in genetics to provide accurate diagnosis and appropriate counseling.

Test Name	DYM Gene Dyggve-Melchior-Clausen disease 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	Metabolic Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for DYM Gene Dyggve-Melchior-Clausen disease NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Dyggve-Melchior-Clausen disease
Test Details	DYM Gene Dyggve-Melchior-Clausen disease NGS Genetic Test is a genetic test that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the DYM gene. This gene is associated with Dyggve-Melchior-Clausen disease, which is a rare genetic disorder characterized by skeletal abnormalities and intellectual disability. The NGS Genetic Test analyzes the DNA of an individual to identify any mutations or variations in the DYM gene that may be responsible for causing the disease. This test can help in confirming a diagnosis of Dyggve-Melchior-Clausen disease and also provide information about the specific mutation present in an individual. The test is usually performed on a blood or saliva sample and involves sequencing the DNA to detect any variations in the DYM gene. The results of the test can help in determining the genetic cause of the disease, predicting the prognosis, and guiding appropriate treatment and management strategies. It is important to note that this test is typically performed in specialized genetic testing laboratories and requires a referral from a healthcare provider or genetic counselor. The test results should be interpreted by a healthcare professional with expertise in genetics to provide accurate diagnosis and appropriate counseling.