📂 Diseases
fibrochondrogenesis — Definition
Fibrokondrogenezis / fibrochondrogenesis
Fibrokondrogenezis is a rare genetic disease characterized by abnormal development of bone and cartilage tissue. This condition leads to shortness, spine deformities and joint abnormalities especially in long bones. The disease shows autozomal resessive inheritance and is often pronounced in prenatal period. Clinical findings include severe skeleton dysplasia, respiratory shortage and facial anomalies.
Frequently Asked Questions
❓ What is Fibrokondrogenezis?
Fibrokondrogenezis; fibrokondrogenezis is a rare genetic disease characterized by abnormal development of bone and cartilage tissue. This condition leads to shortness, spine deformities and joint abnormalities especially in long bones. The disease shows autozomal resessive inheritance and is often pronounced in prenatal period. Clinical findings include severe skeleton dysplasia, respiratory shortage and facial anomalies.
❓ What is fibrochondrogenesis in Turkish?
The Turkish equivalent of "fibrochondrogenesis" is Fibrokondrogenezis.
❓ Which medical field is Fibrokondrogenezis related to?
This term belongs to the Diseases category.