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TMPRSS6 Gene Iron-Refractory Iron Deficiency Anemia Genetic Test

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

-21%

The TMPRSS6 Gene Iron-Refractory Iron Deficiency Anemia Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the TMPRSS6 gene. This gene plays a crucial role in the regulation of iron metabolism in the body. Mutations in the TMPRSS6 gene can lead to Iron-Refractory Iron Deficiency Anemia (IRIDA), a rare and inherited form of anemia that does not respond to oral iron supplements and only partially responds to intravenous iron therapy.

The test is aimed at individuals who exhibit symptoms of iron deficiency anemia that does not improve with standard iron supplementation, suggesting the possibility of an underlying genetic condition like IRIDA. By analyzing the patient’s DNA, the test identifies specific mutations in the TMPRSS6 gene that are responsible for the disorder, thereby facilitating a precise diagnosis.

Conducted at DNA Labs UAE, a facility known for its advanced genetic testing services, the test offers a critical tool for healthcare providers in the management of patients with unexplained iron deficiency anemia. The cost of the test is 4400 AED, reflecting the comprehensive analysis and the specialized technology employed in detecting the genetic mutations associated with this condition.

By confirming a diagnosis of IRIDA, the TMPRSS6 Gene Iron-Refractory Iron Deficiency Anemia Genetic Test enables targeted treatment approaches that can significantly improve patient outcomes. This test represents an important step forward in the personalized treatment of iron deficiency anemia, offering hope to those affected by this challenging condition.

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Genetic Lab Blog – TMPRSS6 Gene Iron-refractory iron deficiency anemia Genetic Test

At DNA Labs UAE, we offer the TMPRSS6 Gene Iron-refractory iron deficiency anemia Genetic Test for the cost of AED 4400.0. This test is used to diagnose iron-refractory iron deficiency anemia, a rare genetic disorder that is characterized by chronic iron deficiency anemia that does not respond to oral iron supplementation.

The test requires a blood sample or extracted DNA, or even just one drop of blood on an FTA Card. The report will be delivered within 3 to 4 weeks using NGS Technology, a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously.

The test is performed by our team of expert hematologists in our Genetics department. Before the test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the TMPRSS6 Gene Iron-refractory iron deficiency anemia NGS Genetic DNA Test gene TMPRSS6.

The TMPRSS6 gene is responsible for encoding a protein called transmembrane protease, serine 6. This protein plays a crucial role in the regulation of iron homeostasis in the body. By analyzing the entire coding region of the TMPRSS6 gene, NGS genetic testing can provide comprehensive information about any genetic changes that may be present.

NGS genetic testing can help confirm a diagnosis of iron-refractory iron deficiency anemia and identify specific mutations that may be causing the disorder. It can also provide information about the inheritance pattern of the disorder. The TMPRSS6 gene mutations associated with iron-refractory iron deficiency anemia can be inherited in an autosomal recessive manner, meaning that both copies of the gene must be affected for the disorder to be present. NGS testing can help determine if an individual carries one or two copies of the mutated gene.

In conclusion, NGS genetic testing for the TMPRSS6 gene is a valuable tool for the diagnosis and management of iron-refractory iron deficiency anemia. It can confirm the diagnosis, identify specific mutations, and provide information about the inheritance pattern of the disorder.

Test Name TMPRSS6 Gene Iron-refractory iron deficiency anemia 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 Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TMPRSS6 Gene Iron-refractory iron deficiency anemia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TMPRSS6 Gene Iron-refractory iron deficiency anemia NGS Genetic DNA Test gene TMPRSS6
Test Details

TMPRSS6 gene is a gene that encodes a protein called transmembrane protease, serine 6. This protein is involved in the regulation of iron homeostasis in the body. Iron-refractory iron deficiency anemia (IRIDA) is a rare genetic disorder characterized by chronic iron deficiency anemia that does not respond to oral iron supplementation.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of IRIDA, NGS genetic testing can be used to identify mutations or variations in the TMPRSS6 gene that may be responsible for the disorder.

By analyzing the entire coding region of the TMPRSS6 gene, NGS genetic testing can provide comprehensive information about any genetic changes that may be present. This can help in confirming a diagnosis of IRIDA and in identifying specific mutations that may be causing the disorder.

NGS genetic testing can also be used to provide information about the inheritance pattern of IRIDA. The TMPRSS6 gene mutations associated with IRIDA can be inherited in an autosomal recessive manner, meaning that both copies of the gene must be affected for the disorder to be present. NGS testing can help determine if an individual carries one or two copies of the mutated gene.

Overall, NGS genetic testing for the TMPRSS6 gene can provide valuable information for the diagnosis and management of iron-refractory iron deficiency anemia. It can help confirm the diagnosis, identify specific mutations, and provide information about the inheritance pattern of the disorder.