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CBL Gene Noonan Syndrome-like Disorder with or without Juvenile Meylomonocytic Leukemia Genetic Test Cost

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

-21%

The CBL Gene Noonan Syndrome-like Disorder with or without Juvenile Myelomonocytic Leukemia Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE. This test is specifically designed to detect mutations in the CBL gene, which are associated with the development of Noonan Syndrome-like disorder, a condition that affects many parts of the body and is characterized by distinctive facial features, heart defects, developmental delays, and other physical problems. Additionally, mutations in the CBL gene can lead to juvenile myelomonocytic leukemia (JMML), a rare and serious form of blood cancer that occurs in young children.

The importance of this test lies in its ability to provide crucial genetic information that can guide the clinical management and treatment plans for affected individuals. Early diagnosis through genetic testing can significantly improve the quality of life for patients by enabling timely interventions and personalized care strategies.

The test is conducted at DNA Labs UAE, a leading facility known for its state-of-the-art genetic testing services. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed reporting provided. This test is a valuable resource for families seeking answers about these complex conditions, offering hope through advanced genetic insights.

Description

CBL Gene Noonan Syndrome-Like Disorder with or without Juvenile Meylomonocytic Leukemia Genetic Test

At DNA Labs UAE, we offer the CBL Gene Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia Genetic Test. This test helps in diagnosing and understanding the genetic components of Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia (JMML).

Test Details

The CBL gene is associated with a disorder called Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia (JMML). This disorder is characterized by developmental delays, distinctive facial features, heart defects, and an increased risk of developing JMML, a rare type of childhood leukemia.

Our genetic testing method, Next-Generation Sequencing (NGS) technology, allows us to analyze multiple genes simultaneously. In the context of CBL gene testing, NGS can identify mutations or variations in the CBL gene that may be responsible for causing the Noonan syndrome-like disorder with or without JMML. This type of genetic testing can help confirm a diagnosis, predict disease progression, assess the risk of developing JMML, and guide treatment decisions.

NGS genetic testing is a non-invasive procedure that requires a blood sample or extracted DNA. Alternatively, one drop of blood on an FTA card can also be used for testing. The test results will be delivered within 3 to 4 weeks.

Pre Test Information

Before undergoing the CBL Gene Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the CBL Gene Noonan syndrome-like disorder with or without JMML.

Test Cost and Doctor

The cost of the CBL Gene Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia Genetic Test is AED 4400.0. This test falls under the genetics department and is recommended for pediatrics. The interpretation of test results should always be done by a qualified healthcare professional.

Conclusion

The CBL Gene Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia Genetic Test is a valuable tool for diagnosing and understanding this rare genetic disorder. It can provide important insights into disease progression, risk assessment, and treatment decisions. Our advanced NGS technology ensures accurate and efficient analysis of the CBL gene. For personalized medical advice and interpretation of test results, it is crucial to consult with a qualified healthcare professional.

Test Name	CBL Gene Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia 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 CBL Gene Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CBL Gene Noonan syndrome-like disorder with or without juvenile meylomonocytic leukemia NGS Genetic DNA Test gene CBL
Test Details	The CBL gene is associated with a disorder called Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia (JMML). This disorder is characterized by developmental delays, distinctive facial features, heart defects, and an increased risk of developing JMML, a rare type of childhood leukemia. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of CBL gene testing, NGS can be used to identify mutations or variations in the CBL gene that may be responsible for causing the Noonan syndrome-like disorder with or without JMML. This type of genetic testing can help in confirming a diagnosis, predicting disease progression, assessing the risk of developing JMML, and guiding treatment decisions. It can also be used for genetic counseling and family planning purposes. It’s important to note that the interpretation of genetic test results should always be done by a qualified healthcare professional who can provide personalized medical advice based on the specific situation and clinical findings of the individual being tested.

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