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GPD1 Gene Hypertriglyceridemia Transient Infantile Genetic Test Cost

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

-21%

The GPD1 gene hypertriglyceridemia transient infantile genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the GPD1 gene. This gene plays a critical role in lipid metabolism, and its mutations are associated with transient infantile hypertriglyceridemia, a rare condition characterized by significantly elevated levels of triglycerides in the blood during infancy. This condition may lead to symptoms such as hepatomegaly (enlarged liver), pancreatitis, and lipid deposits on the skin, although many infants improve as they grow older.

The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities in the GPD1 gene. Identifying these mutations can be crucial for early diagnosis and management of the condition, potentially guiding dietary and medical interventions to prevent or mitigate symptoms and complications associated with high triglyceride levels.

At DNA Labs UAE, the cost of the GPD1 gene hypertriglyceridemia transient infantile genetic test is 4400 AED. This price reflects the comprehensive analysis and detailed reporting that accompanies this specialized genetic test, providing valuable insights for affected families and their healthcare providers.

Description

GPD1 Gene Hypertriglyceridemia Transient Infantile Genetic Test

Test Name: GPD1 Gene Hypertriglyceridemia Transient Infantile 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: Hepatology, Nephrology, Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for GPD1 Gene Hypertriglyceridemia, Transient Infantile NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GPD1 Gene Hypertriglyceridemia, Transient Infantile NGS Genetic DNA Test gene GPD1

Test Details: GPD1 gene hypertriglyceridemia is a genetic disorder characterized by high levels of triglycerides in the blood. It is caused by mutations in the GPD1 gene, which provides instructions for making an enzyme called glycerol-3-phosphate dehydrogenase. Glycerol-3-phosphate dehydrogenase is involved in the breakdown of fats in the body. Mutations in the GPD1 gene can lead to a deficiency or dysfunction of this enzyme, resulting in the accumulation of triglycerides in the blood. A next-generation sequencing (NGS) genetic test can be used to detect mutations in the GPD1 gene. NGS is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes or the entire genome. It can provide comprehensive genetic information and help identify specific mutations that may be causing hypertriglyceridemia. Transient infantile hypertriglyceridemia refers to a temporary increase in triglyceride levels during infancy. It is often associated with certain medical conditions or dietary factors and typically resolves on its own as the child grows older. NGS genetic testing for GPD1 gene hypertriglyceridemia can help in the diagnosis and management of the condition. It can provide valuable information about the specific genetic mutations present, which can guide treatment decisions and help predict the long-term outlook for affected individuals.

Test Name	GPD1 Gene Hypertriglyceridemia transient infantile 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	Hepatology Nephrology Endocrinology Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for GPD1 Gene Hypertriglyceridemia, transient infantile NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GPD1 Gene Hypertriglyceridemia, transient infantile NGS Genetic DNA Test gene GPD1
Test Details	GPD1 gene hypertriglyceridemia is a genetic disorder characterized by high levels of triglycerides in the blood. It is caused by mutations in the GPD1 gene, which provides instructions for making an enzyme called glycerol-3-phosphate dehydrogenase. Glycerol-3-phosphate dehydrogenase is involved in the breakdown of fats in the body. Mutations in the GPD1 gene can lead to a deficiency or dysfunction of this enzyme, resulting in the accumulation of triglycerides in the blood. A next-generation sequencing (NGS) genetic test can be used to detect mutations in the GPD1 gene. NGS is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes or the entire genome. It can provide comprehensive genetic information and help identify specific mutations that may be causing hypertriglyceridemia. Transient infantile hypertriglyceridemia refers to a temporary increase in triglyceride levels during infancy. It is often associated with certain medical conditions or dietary factors and typically resolves on its own as the child grows older. NGS genetic testing for GPD1 gene hypertriglyceridemia can help in the diagnosis and management of the condition. It can provide valuable information about the specific genetic mutations present, which can guide treatment decisions and help predict the long-term outlook for affected individuals.