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SLC40A1 Gene Hemochromatosis Type 4 Genetic Test Cost

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

-21%

The SLC40A1 gene hemochromatosis type 4 genetic test is a specialized diagnostic procedure designed to identify mutations in the SLC40A1 gene, which are linked to a rare form of hereditary hemochromatosis, known as type 4 or ferroportin disease. This condition affects the body’s ability to regulate iron absorption, leading to iron overload and potential damage to organs such as the liver, heart, and pancreas. Early detection through genetic testing is crucial for managing the condition effectively and preventing severe complications.

The test involves collecting a DNA sample, usually through a blood draw, which is then analyzed in a laboratory setting to detect specific genetic mutations in the SLC40A1 gene. The outcome of this test can provide valuable information for individuals with a family history of the condition or those exhibiting symptoms related to iron overload, aiding in the diagnosis and guiding treatment decisions.

Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, the cost of the SLC40A1 gene hemochromatosis type 4 genetic test is set at 4400 AED. The test is performed by qualified professionals who ensure accuracy and confidentiality of the results, providing patients and their families with essential insights into their genetic health and risk factors related to hereditary hemochromatosis type 4.

Description

SLC40A1 Gene Hemochromatosis type 4 Genetic Test

Test Name: SLC40A1 Gene Hemochromatosis type 4 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 SLC40A1 Gene Hemochromatosis type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hemochromatosis type 4.

Test Details: The SLC40A1 gene is responsible for encoding a protein called ferroportin, which is involved in the transport of iron out of cells. Mutations in the SLC40A1 gene can lead to a condition called hemochromatosis type 4, which is a rare form of hereditary hemochromatosis. Hemochromatosis is a disorder characterized by the accumulation of excess iron in the body. In hemochromatosis type 4, mutations in the SLC40A1 gene disrupt the normal function of ferroportin, leading to impaired iron transport and increased iron absorption from the diet. This results in the gradual accumulation of iron in various organs and tissues, including the liver, heart, pancreas, and joints.

NGS (Next-Generation Sequencing) genetic testing is a technique used to sequence multiple genes simultaneously, allowing for the identification of mutations or variations in the SLC40A1 gene associated with hemochromatosis type 4. This type of genetic test can help diagnose individuals with suspected hereditary hemochromatosis and provide information about the specific genetic variant causing the condition.

Genetic testing for hemochromatosis type 4 can be useful for confirming a diagnosis, predicting the risk of developing iron overload-related complications, and guiding treatment strategies. It can also be valuable for identifying at-risk family members who may benefit from early intervention or preventive measures.

It is important to note that genetic testing for hemochromatosis type 4 should be performed and interpreted by a qualified healthcare professional or genetic counselor. They can provide guidance on the implications of test results, discuss treatment options, and offer appropriate genetic counseling to individuals and families affected by this condition.

Test Name	SLC40A1 Gene Hemochromatosis type 4 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 SLC40A1 Gene Hemochromatosis type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hemochromatosis type 4
Test Details	The SLC40A1 gene is responsible for encoding a protein called ferroportin, which is involved in the transport of iron out of cells. Mutations in the SLC40A1 gene can lead to a condition called hemochromatosis type 4, which is a rare form of hereditary hemochromatosis. Hemochromatosis is a disorder characterized by the accumulation of excess iron in the body. In hemochromatosis type 4, mutations in the SLC40A1 gene disrupt the normal function of ferroportin, leading to impaired iron transport and increased iron absorption from the diet. This results in the gradual accumulation of iron in various organs and tissues, including the liver, heart, pancreas, and joints. NGS (Next-Generation Sequencing) genetic testing is a technique used to sequence multiple genes simultaneously, allowing for the identification of mutations or variations in the SLC40A1 gene associated with hemochromatosis type 4. This type of genetic test can help diagnose individuals with suspected hereditary hemochromatosis and provide information about the specific genetic variant causing the condition. Genetic testing for hemochromatosis type 4 can be useful for confirming a diagnosis, predicting the risk of developing iron overload-related complications, and guiding treatment strategies. It can also be valuable for identifying at-risk family members who may benefit from early intervention or preventive measures. It is important to note that genetic testing for hemochromatosis type 4 should be performed and interpreted by a qualified healthcare professional or genetic counselor. They can provide guidance on the implications of test results, discuss treatment options, and offer appropriate genetic counseling to individuals and families affected by this condition.