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CSF3R Gene Neutrophilia Hereditary Genetic Test Cost

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

-21%

The CSF3R gene plays a crucial role in the regulation of granulocyte production and function within the human body. Mutations in the CSF3R gene can lead to hereditary neutrophilia, a condition characterized by an abnormally high number of neutrophils, a type of white blood cell essential for combating infections. Identifying mutations in the CSF3R gene is crucial for diagnosing hereditary neutrophilia, understanding its pathogenesis, and guiding treatment options.

DNA Labs UAE offers a specialized genetic test to detect mutations in the CSF3R gene, aiding in the diagnosis of hereditary neutrophilia. This test is particularly valuable for individuals with a family history of neutrophilia or those exhibiting symptoms related to high neutrophil counts, such as recurrent infections or inflammation. The test cost is set at 4400 AED, reflecting the specialized nature of the analysis and the comprehensive insights it provides into the patient’s genetic makeup concerning the CSF3R gene. By opting for this test at DNA Labs UAE, patients and healthcare providers can make informed decisions regarding the management of hereditary neutrophilia and related conditions.

Description

CSF3R Gene Neutrophilia Hereditary Genetic Test

Test Name: CSF3R Gene Neutrophilia Hereditary 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: Hematology

Doctor: Hematologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for CSF3R Gene Neutrophilia, hereditary NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CSF3R Gene Neutrophilia, hereditary NGS Genetic DNA Test gene CSF3R

Test Details: Neutrophilia refers to an increased number of neutrophils, a type of white blood cell, in the blood. It can be caused by various factors, including infections, inflammation, medications, and certain medical conditions. In some cases, neutrophilia can be hereditary, meaning it is caused by genetic mutations. One genetic mutation associated with hereditary neutrophilia is found in the CSF3R gene. The CSF3R gene provides instructions for making a protein called granulocyte colony-stimulating factor receptor (G-CSFR), which is involved in the production and maturation of neutrophils. Next-generation sequencing (NGS) is a genetic testing method that can be used to analyze the CSF3R gene and identify any mutations or variations present. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variants. A genetic test for CSF3R gene mutations can help in the diagnosis of hereditary neutrophilia. It can also be used to determine the risk of passing on the condition to future generations and guide treatment decisions. It is important to note that hereditary neutrophilia is a rare condition, and the CSF3R gene mutation is just one of several possible genetic causes. Genetic testing should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and counseling.

Test Name	CSF3R Gene Neutrophilia hereditary 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 CSF3R Gene Neutrophilia, hereditary NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CSF3R Gene Neutrophilia, hereditary NGS Genetic DNA Test gene CSF3R
Test Details	Neutrophilia refers to an increased number of neutrophils, a type of white blood cell, in the blood. It can be caused by various factors, including infections, inflammation, medications, and certain medical conditions. In some cases, neutrophilia can be hereditary, meaning it is caused by genetic mutations. One genetic mutation associated with hereditary neutrophilia is found in the CSF3R gene. The CSF3R gene provides instructions for making a protein called granulocyte colony-stimulating factor receptor (G-CSFR), which is involved in the production and maturation of neutrophils. Next-generation sequencing (NGS) is a genetic testing method that can be used to analyze the CSF3R gene and identify any mutations or variations present. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variants. A genetic test for CSF3R gene mutations can help in the diagnosis of hereditary neutrophilia. It can also be used to determine the risk of passing on the condition to future generations and guide treatment decisions. It is important to note that hereditary neutrophilia is a rare condition, and the CSF3R gene mutation is just one of several possible genetic causes. Genetic testing should be conducted by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and counseling.