{"id":11833,"date":"2025-07-25T23:23:41","date_gmt":"2025-07-25T21:23:41","guid":{"rendered":"https:\/\/valintermed.com\/?p=11833"},"modified":"2025-07-25T23:23:41","modified_gmt":"2025-07-25T21:23:41","slug":"dishondrosteoz-leri-veylya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/dishondrosteoz-leri-veylya\/","title":{"rendered":"Leri-Weil's dyschondrosteosis"},"content":{"rendered":"
<\/div>\n

Dyschondrosteosis Leri-Weil is a rare hereditary disease caused by abnormalities in the development of cartilage and bones, which leads to short stature and limb deformities. This disease, named after the French physician Georges Leri and the Swiss pediatrician Alfred Weil, forms part of a group of dysplastic disorders, often accompanied by anomalies of mesenchymal origin. The pathology has a complex multifactorial pathogenesis, including genetic predisposition, which makes its study relevant for specialists in the field of medical genetics and orthopedics. The main mechanism underlying this disease is associated with a violation of cartilaginous metabolic activity, which in turn leads to a change in the shape and functionality of the skeletal system.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n