Short Description

NGS genetic DNA test detecets for variant and mutation detection in FGFR1 gene for Craniosynostosis, FGFR1 related

PreTest Information

Clinical History of Patient who is going for FGFR1 Gene Craniosynostosis, FGFR1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR1 Gene Craniosynostosis, FGFR1 related NGS Genetic DNA Test gene FGFR1

Detail Description

FGFR1 Gene Craniosynostosis | DNA Labs India | NGS Genetic DNA Test

What is FGFR1 Gene Craniosynostosis?

FGFR1 Gene Craniosynostosis is a genetic condition that affects the development of the skull. Craniosynostosis is the premature fusion of the skull bones, which can result in an abnormal head shape and potentially lead to neurological problems. FGFR1 Gene Craniosynostosis is caused by a mutation in the FGFR1 gene, which plays a role in bone development.

NGS Genetic DNA Test for FGFR1 Gene Craniosynostosis

DNA Labs India offers an NGS Genetic DNA Test for the diagnosis of FGFR1 Gene Craniosynostosis. NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that can analyze multiple genes at once. The cost of this test is INR 20000.

Symptoms of FGFR1 Gene Craniosynostosis

The symptoms of FGFR1 Gene Craniosynostosis can vary depending on the severity of the condition. Some common symptoms include:

• Abnormal head shape
• Delayed development
• Seizures
• Visual disturbances
• Intellectual disability

Diagnosis of FGFR1 Gene Craniosynostosis

Diagnosis of FGFR1 Gene Craniosynostosis typically involves a physical examination and imaging tests such as X-rays, CT scans, or MRI scans. Genetic testing, such as the NGS Genetic DNA Test offered by DNA Labs India, can also be used to confirm a diagnosis.