What is osteogenesis imperfecta type 4? Definition, Meaning & Symptoms — Medical Dictionary
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osteogenesis imperfecta type 4 — Definition

Osteogenezis İmperfekta Tip 4 / osteogenesis imperfecta type 4
Osteogenesis imperfekta type 4 is a genetic bond tissue disease, which causes easy fracture of bones. Type 4 is diluted in medium violence and is often pronounced in birth or early childhood. Blue sklera in patients (blueness in the eye flux) is not seen and can be found in dentinogenesis imperfekta (transparent teeth). Fractures often tend to decrease with age, but their size shortness and bone deformities are common.
Turkish
🇹🇷 Osteogenezis İmperfekta Tip 4
English
🇬🇧 osteogenesis imperfecta type 4
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Frequently Asked Questions

❓ What is Osteogenezis İmperfekta Tip 4?
Osteogenezis İmperfekta Tip 4; osteogenesis imperfekta type 4 is a genetic bond tissue disease, which causes easy fracture of bones. Type 4 is diluted in medium violence and is often pronounced in birth or early childhood. Blue sklera in patients (blueness in the eye flux) is not seen and can be found in dentinogenesis imperfekta (transparent teeth). Fractures often tend to decrease with age, but their size shortness and bone deformities are common.
❓ What is osteogenesis imperfecta type 4 in Turkish?
The Turkish equivalent of "osteogenesis imperfecta type 4" is Osteogenezis İmperfekta Tip 4.
❓ Which medical field is Osteogenezis İmperfekta Tip 4 related to?
This term belongs to the Diseases category.