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CBFB Gene Skeletal Abnormalities CBFB Related Genetic Test Cost

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

-21%

The CBFB gene plays a crucial role in the development of bones and certain types of blood cells. Mutations in this gene can lead to skeletal abnormalities, impacting bone formation and structure. These anomalies can range from mild to severe and may affect both the appearance and functionality of the skeletal system. To identify potential mutations in the CBFB gene that could be responsible for these abnormalities, DNA Labs UAE offers a specialized genetic test.

This test is designed to analyze the CBFB gene for any mutations that might be linked to skeletal disorders. It is a valuable diagnostic tool for individuals who exhibit symptoms of skeletal abnormalities or have a family history of such conditions. By pinpointing the exact mutation, healthcare providers can better understand the condition, predict its progression, and tailor treatment plans to manage symptoms effectively.

The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the CBFB gene. Conducted at DNA Labs UAE, the process involves collecting a DNA sample from the patient, typically through a blood draw or cheek swab. The sample is then analyzed in the lab using advanced genetic sequencing techniques.

Overall, the CBFB-related genetic test is a critical resource for individuals and families dealing with skeletal abnormalities, offering insights that can guide diagnosis, treatment, and management of these complex conditions.

Description

CBFB Gene Skeletal Abnormalities – Genetic Test

At DNA Labs UAE, we offer a comprehensive genetic test for CBFB gene skeletal abnormalities. This test can help diagnose and provide valuable information on the underlying genetic cause of skeletal abnormalities related to the CBFB gene.

Test Name: CBFB Gene Skeletal Abnormalities CBFB Related 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: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics

Pre Test Information

Before undergoing the CBFB gene skeletal abnormalities genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by CBFB gene skeletal abnormalities.

Test Details

The CBFB gene, also known as core-binding factor subunit beta, plays a crucial role in normal skeletal development. Mutations in this gene can lead to skeletal abnormalities. To diagnose CBFB-related skeletal abnormalities, we utilize a genetic test called Next-Generation Sequencing (NGS).

NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of CBFB gene testing, it can identify mutations or variations in the CBFB gene that may be causing the skeletal abnormalities.

The genetic test involves extracting DNA from a patient’s blood or other tissue sample. The DNA is then sequenced using NGS technology, which generates a large amount of data. This data is carefully analyzed to identify any variations or mutations in the CBFB gene that may be associated with skeletal abnormalities.

Genetic testing for CBFB-related skeletal abnormalities is essential for accurate diagnosis, providing information on the underlying genetic cause, and guiding treatment and management options. It can also be valuable for genetic counseling and family planning purposes.

It is important to note that genetic testing should always be performed by qualified healthcare professionals who specialize in genetics. They have the expertise to accurately interpret the test results and provide appropriate counseling.

At DNA Labs UAE, we are committed to delivering accurate and reliable genetic testing services. Our team of experts in genetics and pediatrics is dedicated to helping individuals and families understand and manage genetic conditions.

Test Name	CBFB Gene Skeletal abnormalities CBFB related 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	Dysmorphology
Doctor	Pediatrics
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for CBFB Gene Skeletal abnormalities, CBFB related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CBFB Gene Skeletal abnormalities, CBFB related NGS Genetic DNA Test gene CBFB
Test Details	The CBFB gene, also known as core-binding factor subunit beta, is involved in normal skeletal development. Mutations in this gene can lead to skeletal abnormalities. To diagnose CBFB-related skeletal abnormalities, a genetic test called Next-Generation Sequencing (NGS) can be used. NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes or even the entire genome. It can identify mutations or variations in the CBFB gene that may be causing the skeletal abnormalities. NGS-based genetic testing involves extracting DNA from a patient’s blood or other tissue sample. The DNA is then sequenced using NGS technology, which generates a large amount of data. This data is then analyzed to identify any variations or mutations in the CBFB gene that may be associated with skeletal abnormalities. Genetic testing for CBFB-related skeletal abnormalities can help in diagnosing the condition, providing information on the underlying genetic cause, and guiding treatment and management options. It can also be useful for genetic counseling and family planning purposes. It is important to note that genetic testing should be performed by qualified healthcare professionals who specialize in genetics, as they can provide accurate interpretation of the test results and appropriate counseling.

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