📂 Diseases
osteogenesis imperfecta type 11 — Definition
Osteogenezis İmperfekta Tip 11 / osteogenesis imperfecta type 11
Osteogenesis imperfekta type 11, is a rare genetic bond tissue disease characterized by excessive brittleness and deformities of bones. This type is caused by mutations in the FKBP10 gene, which is mainly involved in bone mineralization. Results such as frequent fractures, short size, scoliosis and respiratory problems can be seen in patients. Otozomal indicates a paterni of resesif inheritance and can monitor a more severe clinical cruise compared to other types.
Frequently Asked Questions
❓ What is Osteogenezis İmperfekta Tip 11?
Osteogenezis İmperfekta Tip 11; osteogenesis imperfekta type 11, is a rare genetic bond tissue disease characterized by excessive brittleness and deformities of bones. This type is caused by mutations in the FKBP10 gene, which is mainly involved in bone mineralization. Results such as frequent fractures, short size, scoliosis and respiratory problems can be seen in patients. Otozomal indicates a paterni of resesif inheritance and can monitor a more severe clinical cruise compared to other types.
❓ What is osteogenesis imperfecta type 11 in Turkish?
The Turkish equivalent of "osteogenesis imperfecta type 11" is Osteogenezis İmperfekta Tip 11.
❓ Which medical field is Osteogenezis İmperfekta Tip 11 related to?
This term belongs to the Diseases category.