{"id":11288,"date":"2025-07-27T02:27:01","date_gmt":"2025-07-27T00:27:01","guid":{"rendered":"https:\/\/valintermed.com\/?p=11288"},"modified":"2025-07-27T02:27:01","modified_gmt":"2025-07-27T00:27:01","slug":"fibrohondrogenez","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/fibrochondrogenesis\/","title":{"rendered":"Fibrochondrogenesis"},"content":{"rendered":"
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Fibrochondrogenesis is a rare and hereditary disease characterized by abnormal development of cartilage and connective tissue. It belongs to the group of dysplasias, which leads to multiple disorders in the formation of the skeleton, especially in the area of cartilage and joints. Based on mutations in genes responsible for the proliferation and metabolism of cartilage tissue, they manifest clinically in the form of limb deformities, growth disorders, and possible involvement of internal organs. The severity of symptoms can vary from mild dysplasia to severe forms with multiple anomalies affecting the respiratory and cardiovascular systems.<\/p>\n

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