Stuve-Wiedemann Syndrome is a rare genetic disorder characterized by skeletal abnormalities and muscle weakness. It is not contagious and cannot be transmitted from person to person. This condition is caused by mutations in the LIFR gene and is inherited in an autosomal recessive manner. Stuve-Wiedemann Syndrome affects individuals regardless of their gender or ethnicity. Early diagnosis and appropriate medical management are crucial in improving the quality of life for individuals with this syndrome.