📂 Diseases
osteogenesis imperfecta type 13 — Definition
Osteogenezis İmperfekta Tip 13 / osteogenesis imperfecta type 13
Osteogenesis imperfekta type 13, is a rare genetic disease characterized by excessive brittleness and deformities of bones. This type is usually caused by mutations in BMP1 gene and leads to disorder in collagen synthesis. Results such as frequent fractures, short size, blue sklera and dental anomalies can be seen in patients. Otozomal shows a paterni of resesif inheritance and is observed in milder to medium violence compared to other types.
Frequently Asked Questions
❓ What is Osteogenezis İmperfekta Tip 13?
Osteogenezis İmperfekta Tip 13; osteogenesis imperfekta type 13, is a rare genetic disease characterized by excessive brittleness and deformities of bones. This type is usually caused by mutations in BMP1 gene and leads to disorder in collagen synthesis. Results such as frequent fractures, short size, blue sklera and dental anomalies can be seen in patients. Otozomal shows a paterni of resesif inheritance and is observed in milder to medium violence compared to other types.
❓ What is osteogenesis imperfecta type 13 in Turkish?
The Turkish equivalent of "osteogenesis imperfecta type 13" is Osteogenezis İmperfekta Tip 13.
❓ Which medical field is Osteogenezis İmperfekta Tip 13 related to?
This term belongs to the Diseases category.