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FANCM Gene Fanconi anemia type M Genetic Test Cost

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

-21%

The FANCM gene is associated with Fanconi anemia type M, a rare genetic disorder that affects the bone marrow and results in decreased production of all types of blood cells. This condition can lead to physical abnormalities, organ defects, and an increased risk of certain cancers. The FANCM gene plays a crucial role in the body’s ability to repair damaged DNA, and mutations in this gene can disrupt this critical process, leading to the symptoms and complications associated with Fanconi anemia.

To diagnose Fanconi anemia type M and identify mutations in the FANCM gene, a genetic test is available at DNA Labs UAE. This test involves analyzing the patient’s DNA to look for mutations in the FANCM gene that are known to cause the condition. It is a vital tool for confirming the diagnosis, understanding the disease’s progression, and making informed decisions about treatment options.

The cost of the FANCM gene Fanconi anemia type M genetic test at DNA Labs UAE is 4400 AED. This test is crucial for individuals with a family history of Fanconi anemia or those presenting symptoms consistent with the disorder. By identifying the specific genetic mutation, healthcare providers can offer personalized care and management strategies to improve the quality of life for affected individuals.

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FANCM Gene Fanconi Anemia Type M Genetic Test

Welcome to DNA Labs UAE, where we offer the FANCM Gene Fanconi Anemia Type M Genetic Test. This test is designed to diagnose and provide valuable information about Fanconi anemia type M, a rare genetic disorder characterized by bone marrow failure, physical abnormalities, and an increased risk of developing cancer.

Test Details

The FANCM gene is associated with Fanconi anemia type M. Our genetic testing method, Next-Generation Sequencing (NGS), allows for the simultaneous analysis of multiple genes, including the FANCM gene, to identify any variations or mutations that may be present. This test can help confirm a diagnosis of Fanconi anemia type M in individuals suspected of having the condition. It can also be used for carrier testing to determine if an individual carries a mutation in the FANCM gene and may pass it on to their children.

Components and Price

The FANCM Gene Fanconi Anemia Type M Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Once the sample is collected, the report will be delivered within 3 to 4 weeks.

Method

The FANCM Gene Fanconi Anemia Type M Genetic Test utilizes NGS technology for sequencing and analysis.

Test Type

This test falls under the category of Metabolic Disorders.

Doctor and Test Department

The FANCM Gene Fanconi Anemia Type M Genetic Test is performed under the guidance of a General Physician and is conducted in our Genetics Test Department.

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the FANCM Gene Fanconi Anemia Type M NGS Genetic DNA Test. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by Fanconi anemia type M.

It is crucial to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on the individual’s specific situation.

Test Name FANCM Gene Fanconi anemia type M 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 FANCM Gene Fanconi anemia type M NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type M
Test Details

The FANCM gene is associated with Fanconi anemia type M, a rare genetic disorder characterized by bone marrow failure, physical abnormalities, and an increased risk of developing cancer. NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the FANCM gene, to identify any variations or mutations that may be present.

NGS genetic testing for the FANCM gene can help confirm a diagnosis of Fanconi anemia type M in individuals suspected of having the condition. It can also be used for carrier testing to determine if an individual carries a mutation in the FANCM gene and may pass it on to their children.

The test involves collecting a DNA sample, typically through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to identify any variations or mutations in the FANCM gene. The results of the test can provide valuable information for diagnosis, prognosis, and genetic counseling.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on the individual’s specific situation.

SKU: TEST-2314 Category:

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