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DMGDH Gene Dimethylglycine dehydrogenase deficiency Genetic Test Cost

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

-21%

The DMGDH gene is responsible for encoding the enzyme dimethylglycine dehydrogenase, which plays a crucial role in the metabolism of choline-derived compounds. Deficiency in this enzyme leads to a rare metabolic disorder characterized by elevated levels of dimethylglycine in the blood. This condition can result in a variety of symptoms, including developmental delays, muscular hypotonia, and in some cases, seizures.

To diagnose this condition, a genetic test can be performed that specifically looks for mutations in the DMGDH gene. This test is critical for confirming the diagnosis, understanding the severity of the enzyme deficiency, and guiding treatment plans. It involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for mutations in the DMGDH gene.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test for DMGDH gene deficiency. The cost of the test is 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by professionals with expertise in genetic testing, ensuring accurate and reliable results. This test is a valuable resource for families seeking answers to unexplained symptoms related to metabolic disorders and provides a foundation for personalized treatment strategies.

Description

DMGDH Gene Dimethylglycine dehydrogenase deficiency Genetic Test

Components: DMGDH gene

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 DMGDH Gene Dimethylglycine dehydrogenase deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Dimethylglycine dehydrogenase deficiency.

Test Details:

DMGDH gene, also known as dimethylglycine dehydrogenase gene, is responsible for the production of the enzyme dimethylglycine dehydrogenase. This enzyme plays a crucial role in the metabolism of dimethylglycine (DMG), an amino acid derivative found in the body.

A deficiency in DMGDH gene leads to a condition called dimethylglycine dehydrogenase deficiency (DMGDH deficiency). This is a rare autosomal recessive disorder characterized by the impaired breakdown of DMG, resulting in the accumulation of DMG in the body.

NGS genetic testing, also known as next-generation sequencing, is a high-throughput DNA sequencing technology that allows the simultaneous sequencing of multiple genes or even the entire genome. In the context of DMGDH deficiency, NGS genetic testing can be used to identify mutations or variations in the DMGDH gene that may be responsible for the disorder.

By analyzing the DNA sequence of the DMGDH gene, NGS genetic testing can provide valuable information about the presence of any mutations or variations that may be causing DMGDH deficiency. This information can help in confirming a diagnosis, predicting the severity of the condition, and guiding appropriate treatment and management strategies.

It is important to note that NGS genetic testing for DMGDH deficiency is typically performed in specialized genetic testing laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetics. The results of the genetic test should be interpreted in the context of the individual’s clinical presentation and family history to provide accurate diagnosis and appropriate management.

Test Name	DMGDH Gene Dimethylglycine dehydrogenase deficiency 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 DMGDH Gene Dimethylglycine dehydrogenase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Dimethylglycine dehydrogenase deficiency
Test Details	DMGDH gene, also known as dimethylglycine dehydrogenase gene, is responsible for the production of the enzyme dimethylglycine dehydrogenase. This enzyme plays a crucial role in the metabolism of dimethylglycine (DMG), an amino acid derivative found in the body. A deficiency in DMGDH gene leads to a condition called dimethylglycine dehydrogenase deficiency (DMGDH deficiency). This is a rare autosomal recessive disorder characterized by the impaired breakdown of DMG, resulting in the accumulation of DMG in the body. NGS genetic testing, also known as next-generation sequencing, is a high-throughput DNA sequencing technology that allows the simultaneous sequencing of multiple genes or even the entire genome. In the context of DMGDH deficiency, NGS genetic testing can be used to identify mutations or variations in the DMGDH gene that may be responsible for the disorder. By analyzing the DNA sequence of the DMGDH gene, NGS genetic testing can provide valuable information about the presence of any mutations or variations that may be causing DMGDH deficiency. This information can help in confirming a diagnosis, predicting the severity of the condition, and guiding appropriate treatment and management strategies. It is important to note that NGS genetic testing for DMGDH deficiency is typically performed in specialized genetic testing laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetics. The results of the genetic test should be interpreted in the context of the individual’s clinical presentation and family history to provide accurate diagnosis and appropriate management.