Short Description

NGS genetic DNA test detecets for variant and mutation detection in FGFR3 gene for Crouzon syndrome with acanthosis nigricans

PreTest Information

Clinical History of Patient who is going for FGFR3 Gene Crouzon syndrome with acanthosis nigricans NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR3 Gene Crouzon syndrome with acanthosis nigricans NGS Genetic DNA Test gene FGFR3

Detail Description

FGFR3 Gene Crouzon Syndrome with Acanthosis Nigricans NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis

Are you or someone you know experiencing symptoms of Crouzon Syndrome with Acanthosis Nigricans? DNA Labs India offers NGS Genetic DNA testing for the FGFR3 gene, which can help diagnose this condition. This blog will cover the symptoms, diagnosis, and cost of this test.

What is Crouzon Syndrome with Acanthosis Nigricans?

Crouzon Syndrome is a rare genetic disorder that affects the growth and development of the skull and face. Acanthosis Nigricans is a skin condition characterized by dark, thickened patches of skin. When these two conditions occur together, it is known as Crouzon Syndrome with Acanthosis Nigricans.

Symptoms of Crouzon Syndrome with Acanthosis Nigricans

The symptoms of this condition can vary from person to person, but some common symptoms include:

• Abnormal facial features, such as bulging eyes or a beaked nose
• Craniosynostosis, which is the premature fusion of skull bones
• Underdeveloped midface
• Speech and hearing problems
• Delayed development
• Obstructive sleep apnea
• Acanthosis Nigricans

Diagnosis of Crouzon Syndrome with Acanthosis Nigricans

Diagnosing Crouzon Syndrome with Acanthosis Nigricans usually involves a physical examination, medical history, and genetic testing. The genetic test for this condition looks for mutations in the FGFR3 gene. This gene is responsible for providing instructions to create a protein that is involved in the development and growth of bones and other tissues. Mutations in this gene can cause abnormal bone growth and development, which can lead to the symptoms of Crouzon Syndrome with Acanthosis Nigricans.

NGS Genetic DNA Testing for FGFR3 Gene

DNA Labs India offers NGS Genetic DNA testing for the FGFR3 gene. This test is performed using next-generation sequencing technology, which allows for a more detailed analysis of the gene. The test can identify mutations in the FGFR3 gene that are associated with Crouzon Syndrome with Acanthosis Nigricans. The cost of this test is INR 20000.

Conclusion

Crouzon Syndrome with Acanthosis Nigricans is a rare genetic disorder that can cause a variety of symptoms, including abnormal facial features and skin patches. DNA Labs India offers NGS Genetic DNA testing for the FGFR3 gene, which can help diagnose this condition. If you or someone you know is experiencing symptoms of Crouzon Syndrome with Acanthosis Nigricans, consider getting tested to help with diagnosis and treatment.