FGFR2 Gene Antley-Bixler Syndrome Genetic Test
Are you looking for a reliable genetic lab in UAE that offers the FGFR2 Gene Antley-Bixler Syndrome Genetic Test? Look no further than DNA Labs UAE! We provide comprehensive genetic testing services to help individuals and families understand their genetic makeup.
Test Components and Price
Our FGFR2 Gene Antley-Bixler Syndrome Genetic Test is priced at 4400.0 AED. The test requires a sample condition of blood or extracted DNA, or one drop of blood on an FTA card. The report delivery time is approximately 3 to 4 weeks. We utilize NGS technology, which stands for Next-Generation Sequencing, to conduct this test. The test falls under the dysmorphology category and is conducted by our expert team of pediatricians in our Genetics department.
Pre Test Information and Genetic Counseling
Prior to undergoing the FGFR2 Gene Antley-Bixler Syndrome Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected by the FGFR2 gene. Our genetic counselors are highly experienced and will guide you through the process, ensuring you have a clear understanding of the test and its implications.
About the Test
The FGFR2 gene plays a crucial role in the production of a protein called fibroblast growth factor receptor 2. Mutations in this gene can lead to Antley-Bixler syndrome, a rare genetic disorder that affects multiple systems in the body. Symptoms of this syndrome include craniofacial abnormalities, joint contractures, limb abnormalities, genitourinary malformations, and hearing loss.
Our NGS genetic testing utilizes advanced sequencing technology to analyze multiple genes simultaneously, including the FGFR2 gene. By detecting variations or mutations in this gene, we can confirm a diagnosis of Antley-Bixler syndrome. To conduct the test, we obtain a DNA sample, usually through a blood or saliva sample, which is then sequenced to identify any variations or mutations.
Benefits and Guidance
The results of the FGFR2 Gene Antley-Bixler Syndrome Genetic Test provide valuable information for diagnosis, genetic counseling, and potential treatment options. It is important to note that this test should only be conducted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can interpret the results and provide appropriate guidance and support.
At DNA Labs UAE, we prioritize accuracy, confidentiality, and exceptional patient care. Our team of experts is dedicated to helping you gain insights into your genetic makeup and making informed decisions about your health. Contact us today to schedule your FGFR2 Gene Antley-Bixler Syndrome Genetic Test!
| Test Name | FGFR2 Gene Antley-Bixler syndrome 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 FGFR2 Gene Antley-Bixler syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Antley-Bixler syndrome NGS Genetic DNA Test gene FGFR2 |
| Test Details |
The FGFR2 gene is responsible for providing instructions for making a protein called fibroblast growth factor receptor 2. Mutations in this gene can lead to a condition called Antley-Bixler syndrome. Antley-Bixler syndrome is a rare genetic disorder that affects multiple systems in the body. It is characterized by craniofacial abnormalities, such as craniosynostosis (premature fusion of the skull bones), midface hypoplasia (underdevelopment of the middle part of the face), and proptosis (bulging eyes). Other features of the syndrome may include joint contractures, limb abnormalities, genitourinary malformations, and hearing loss. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. It allows for the detection of mutations or variations in the FGFR2 gene, which can help confirm a diagnosis of Antley-Bixler syndrome. NGS genetic testing involves obtaining a DNA sample, usually through a blood sample or saliva sample. The DNA is then sequenced to identify any variations or mutations in the FGFR2 gene. The results of the test can provide valuable information for diagnosis, genetic counseling, and potential treatment options. It is important to note that genetic testing for Antley-Bixler syndrome should be conducted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can interpret the results and provide appropriate guidance and support. |
