Leary-Weill Dyschondrosteosis

Leri Veilja Dyschondrosis is a rare hereditary disease that is characterized by multiple abnormalities of the bones and cartilage of the skeleton. This disease was named after two famous scientists, Louis Lieri and Jean Weil, who contributed to its research.

Leri Weil Dyschondrotostososis usually appears in adolescence, but can also occur in adults. The main symptom is deformation of bones and joints, which can

Lery-Weil dyschondrostosis is a rare hereditary disease that manifests itself in the form of abnormal bone growth. It occurs due to a violation of the development of cartilage tissue, which is the basis for bones.

Lery-Weil dyschondrostosis can manifest itself in various forms, but the most common is cranial dysplasia. It is characterized by abnormal growth of the skull bones, which can lead to deformation of the face and head.

Treatment for Leri-Weili dyschondrostosis depends on the severity of the disease and may include surgery, orthopedic correction and drug therapy.

It is important to note that Leri-Weil dyschondrostosis is a genetic disease, so parents should be aware of its possible consequences and take preventive measures.