📂 Diseases
osteogenesis imperfecta type 10 — Definition
Osteogenezis İmperfekta Tip 10 / osteogenesis imperfecta type 10
Osteogenesis imperfekta type 10 is a rare genetic bond tissue disease characterized by brittleness and easy fracture of bones. This type is caused by mutations in the SERPINF1 gene and shows autozomal resesif inheritance. Frequent bone fractures in patients, deformities, blue sklera and dental anomalies (dentinogenezis imperfekta) can be seen; but it can be lighter looking than other types in type 10.
Frequently Asked Questions
❓ What is Osteogenezis İmperfekta Tip 10?
Osteogenezis İmperfekta Tip 10; osteogenesis imperfekta type 10 is a rare genetic bond tissue disease characterized by brittleness and easy fracture of bones. This type is caused by mutations in the SERPINF1 gene and shows autozomal resesif inheritance. Frequent bone fractures in patients, deformities, blue sklera and dental anomalies (dentinogenezis imperfekta) can be seen; but it can be lighter looking than other types in type 10.
❓ What is osteogenesis imperfecta type 10 in Turkish?
The Turkish equivalent of "osteogenesis imperfecta type 10" is Osteogenezis İmperfekta Tip 10.
❓ Which medical field is Osteogenezis İmperfekta Tip 10 related to?
This term belongs to the Diseases category.