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HBG2 Gene Cyanosis Transient Neonatal Genetic Test Cost

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

-21%

The “HBG2 Gene Cyanosis Transient Neonatal Genetic Test” is a specialized diagnostic procedure designed to identify genetic mutations in the HBG2 gene, which are associated with transient neonatal cyanosis. Cyanosis refers to a bluish or purplish coloration of the skin and mucous membranes, a condition that is caused by a lack of oxygen in the blood. In newborns, this can be a transient condition, often linked to genetic factors, specifically mutations in the HBG2 gene.

This genetic test involves analyzing the DNA of the newborn to detect any anomalies in the HBG2 gene that could be responsible for the transient cyanosis. Early identification of these mutations allows for prompt and appropriate medical interventions, potentially reducing the risk of complications and guiding the management of the condition.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is set at 4400 AED, reflecting the intricate technology and expertise required to accurately identify mutations in the HBG2 gene. By opting for this test, parents can gain valuable insights into the genetic factors contributing to their newborn’s health condition, enabling informed decisions regarding their child’s care and treatment.

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HBG2 Gene Cyanosis Transient Neonatal Genetic Test

Introduction

The HBG2 gene is responsible for producing a protein called hemoglobin gamma-G. Hemoglobin is a protein found in red blood cells that carries oxygen throughout the body. Mutations in the HBG2 gene can lead to a condition called cyanosis. Cyanosis is a bluish discoloration of the skin and mucous membranes due to a lack of oxygen in the blood. It can be caused by various conditions, including heart defects, lung diseases, and certain genetic disorders. Transient neonatal cyanosis refers to a temporary episode of cyanosis that occurs in newborns. It is often due to a delay in the transition from fetal to adult hemoglobin production.

Test Details

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It can be used to identify genetic mutations or variations that may be associated with certain diseases or conditions. In the context of transient neonatal cyanosis, NGS genetic testing can be used to analyze the HBG2 gene and other relevant genes involved in the production of hemoglobin. This can help identify any mutations or variations that may be contributing to the cyanosis episode.

Test Components and Price

  • Test Name: HBG2 Gene Cyanosis Transient Neonatal Genetic Test
  • 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 HBG2 Gene Cyanosis, transient neonatal NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HBG2 Gene Cyanosis, transient neonatal NGS Genetic DNA Test gene HBG2.

Conclusion

By identifying specific genetic factors, NGS genetic testing can provide valuable information for diagnosing and managing transient neonatal cyanosis. It can help guide appropriate medical interventions and genetic counseling for affected individuals and their families.

Test Name HBG2 Gene Cyanosis transient neonatal 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 HBG2 Gene Cyanosis, transient neonatal NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HBG2 Gene Cyanosis, transient neonatal NGS Genetic DNA Test gene HBG2
Test Details

The HBG2 gene is responsible for producing a protein called hemoglobin gamma-G. Hemoglobin is a protein found in red blood cells that carries oxygen throughout the body. Mutations in the HBG2 gene can lead to a condition called cyanosis.

Cyanosis is a bluish discoloration of the skin and mucous membranes due to a lack of oxygen in the blood. It can be caused by various conditions, including heart defects, lung diseases, and certain genetic disorders.

Transient neonatal cyanosis refers to a temporary episode of cyanosis that occurs in newborns. It is often due to a delay in the transition from fetal to adult hemoglobin production. During fetal development, the predominant form of hemoglobin is fetal hemoglobin (HbF), which has a higher affinity for oxygen than adult hemoglobin (HbA). After birth, there is a gradual switch from producing HbF to HbA.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It can be used to identify genetic mutations or variations that may be associated with certain diseases or conditions.

In the context of transient neonatal cyanosis, NGS genetic testing can be used to analyze the HBG2 gene and other relevant genes involved in the production of hemoglobin. This can help identify any mutations or variations that may be contributing to the cyanosis episode.

By identifying specific genetic factors, NGS genetic testing can provide valuable information for diagnosing and managing transient neonatal cyanosis. It can help guide appropriate medical interventions and genetic counseling for affected individuals and their families.

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