DPM3 Gene Glycosylation Disorder Type 1O Genetic Test sale cost 4400 AED
GYG1 Gene Glycogen storage disease type 15 Genetic Test sale cost 4400 AED GYG1 Gene Glycogen storage disease type 15 Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
SLC35A2 Gene Glycosylation Disorder Type 2M Genetic Test sale cost 4400 AED SLC35A2 Gene Glycosylation Disorder Type 2M 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!

DPM3 Gene Glycosylation Disorder Type 1O Genetic Test Cost

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

-21%

The DPM3 Gene Glycosylation Disorder Type 1O Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the DPM3 gene. These mutations are responsible for a rare congenital disorder known as Congenital Disorder of Glycosylation Type Io (CDG-Io), which affects the body’s ability to properly glycosylate proteins and lipids, essential processes for normal cellular function.

Glycosylation disorders like CDG-Io can lead to a wide range of symptoms, including developmental delay, neurological issues, and abnormalities in various organs. Early and accurate diagnosis through genetic testing can be crucial for managing the condition, offering insights into potential treatments, and guiding family planning decisions.

The test is priced at 4400 AED and is conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services. The process involves collecting a DNA sample from the patient, usually through a blood draw, which is then analyzed for the specific mutations in the DPM3 gene that are indicative of CDG-Io. This test is a vital resource for families seeking answers about this rare genetic disorder and looking for ways to manage its effects.

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

DPM3 Gene Glycosylation Disorder Type 1O Genetic Test

At DNA Labs UAE, we offer the DPM3 Gene Glycosylation Disorder Type 1O Genetic Test to help diagnose and manage this specific subtype of glycosylation disorder. This genetic test analyzes the DPM3 gene and other genes associated with glycosylation disorders using Next-Generation Sequencing (NGS) technology.

Test Details

The DPM3 gene encodes an enzyme called dolichyl-phosphate mannosyltransferase subunit 3, which is involved in the glycosylation process. Glycosylation disorders are genetic disorders that occur due to abnormalities in the glycosylation process, affecting various organs and systems in the body.

Symptoms and Diagnosis

DPM3 gene glycosylation disorder type 1O is characterized by intellectual disability, developmental delay, seizures, and other neurological symptoms. To diagnose this disorder, a patient’s clinical history is taken into consideration. A genetic counseling session is conducted to draw a pedigree chart of affected family members, which helps in understanding the inheritance pattern and identifying individuals at risk.

Test Components and Price

  • Components: DPM3 gene and other genes associated with glycosylation disorders
  • Price: 4400.0 AED

Sample Condition and Report Delivery

  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks

Method and Test Type

  • Method: NGS Technology
  • Test Type: Metabolic Disorders

Doctor and Test Department

  • Doctor: General Physician
  • Test Department: Genetics

Importance of Genetic Counseling

Genetic counseling is an essential part of the testing process for DPM3 gene glycosylation disorder type 1O. It helps individuals understand the inheritance pattern, identify family members at risk, and make informed decisions about family planning and genetic testing.

By undergoing the DPM3 Gene Glycosylation Disorder Type 1O Genetic Test, healthcare professionals can diagnose this disorder accurately and provide appropriate management and treatment options for affected individuals.

Test Name DPM3 Gene Glycosylation disorder type 1O 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 DPM3 Gene Glycosylation disorder type 1O NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glycosylation disorder type 1O
Test Details

The DPM3 gene is responsible for encoding an enzyme called dolichyl-phosphate mannosyltransferase subunit 3. This enzyme is involved in the glycosylation process, which is the attachment of sugar molecules to proteins and lipids.

Glycosylation disorders are a group of genetic disorders that result from abnormalities in the glycosylation process. These disorders can affect various organs and systems in the body, leading to a wide range of symptoms and complications.

DPM3 gene glycosylation disorder type 1O is a specific subtype of glycosylation disorder caused by mutations in the DPM3 gene. This disorder is characterized by intellectual disability, developmental delay, seizures, and other neurological symptoms.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the analysis of multiple genes simultaneously. It uses high-throughput sequencing technologies to rapidly sequence large amounts of DNA. NGS genetic testing can be used to identify mutations in the DPM3 gene and other genes associated with glycosylation disorders.

By performing an NGS genetic test, healthcare professionals can diagnose DPM3 gene glycosylation disorder type 1O and provide appropriate management and treatment options for affected individuals.

SKU: TEST-2385 Category:

Related products