Short Description

NGS genetic DNA test detecets for variant and mutation detection in FGFR3 gene for Hypochondroplasia

PreTest Information

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

Detail Description

FGFR3 Gene Hypochondroplasia NGS Genetic DNA Test cost INR:20000 symptoms diagnosis

FGFR3 gene hypochondroplasia is a rare genetic disorder that affects bone growth. It is caused by mutations in the FGFR3 gene, which provides instructions for making a protein involved in the growth and development of bones.

Some common symptoms of FGFR3 gene hypochondroplasia include short stature, shortening of the limbs, and a large head with a prominent forehead. Other symptoms may include a broad, flat nose, a small jaw, and a curved spine.

If you or your child are experiencing these symptoms, it is important to see a doctor for diagnosis. A genetic DNA test can be performed to confirm the diagnosis and identify the specific FGFR3 gene mutation causing the disorder.

DNA Labs India offers advanced genetic testing services, including the FGFR3 Gene Hypochondroplasia NGS Genetic DNA Test, at an affordable cost of INR:20000. Our team of experienced geneticists and counselors provide accurate and reliable results, along with guidance on treatment options.

With early diagnosis and treatment, individuals with FGFR3 gene hypochondroplasia can lead healthy and fulfilling lives. Contact DNA Labs India today to schedule a genetic DNA test and get started on the path to better health.