📂 Diseases
osteogenesis imperfecta type 19 — Definition
Osteogenezis İmperfekta Tip 19 / osteogenesis imperfecta type 19
Osteogenesis imperfekta type 19, is a rare genetic disorder characterized by excessive brittleness of bones. This type is often associated with bone deformities in mild to medium violence and blue sklera (the blue appearance of the eyelid). The disease is caused by mutations in genes playing a role in bone mineralization and indicates autozomal resesif inheritance.
Frequently Asked Questions
❓ What is Osteogenezis İmperfekta Tip 19?
Osteogenezis İmperfekta Tip 19; osteogenesis imperfekta type 19, is a rare genetic disorder characterized by excessive brittleness of bones. This type is often associated with bone deformities in mild to medium violence and blue sklera (the blue appearance of the eyelid). The disease is caused by mutations in genes playing a role in bone mineralization and indicates autozomal resesif inheritance.
❓ What is osteogenesis imperfecta type 19 in Turkish?
The Turkish equivalent of "osteogenesis imperfecta type 19" is Osteogenezis İmperfekta Tip 19.
❓ Which medical field is Osteogenezis İmperfekta Tip 19 related to?
This term belongs to the Diseases category.