Weismann-Netter syndrome

Weismann-Netter syndrome is a rare genetic condition that affects the bones. It is known as a primary bent bone dysplasia. People with this condition experience abnormal bending of the long bones in their lower legs, with the tibia and fibula showing anterior bowing. The fibula may also be broader and have a thicker back side. These bone changes are accompanied by a short stature and can affect other parts of the skeleton. Additional features can include abnormal spinal curvature such as scoliosis with a pronounced lumbar curve, unusual shape of the sacrum and pelvis, and sometimes irregularities in the vertebrae. Other skeletal differences may include changes in the shape of the clavicles, ribs, and skull bone thickening. Delays in walking and eruption of permanent teeth are also seen in some cases.

People with this condition may have notable bending in the lower leg bones, which leads to difficulty with walking and delayed ambulation. Other common signs include short stature, abnormal spinal curvature like scoliosis with a pronounced lumbar curve, and additional skeletal abnormalities such as a horizontal sacrum and changes in the shape of the pelvis, clavicles, and ribs. There may also be delayed dental development with later eruption of permanent teeth.

Weismann-Netter syndrome is a genetic condition. Although it is known to be inherited, specific gene changes have not been identified in the provided information.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research is currently limited for this condition.