What is Levy-Yeboa Syndrome

Levy-Yeboa Syndrome is a rare genetic disorder that affects the development of various parts of the body. It is characterized by intellectual disability, distinctive facial features, and skeletal abnormalities. This condition is caused by mutations in the SMC1A gene, which plays a crucial role in the normal functioning of cells.

Individuals with Levy-Yeboa Syndrome typically have moderate to severe intellectual disability, with delayed speech and language development. They may also exhibit distinctive facial features such as a prominent forehead, widely spaced eyes, and a small chin. Skeletal abnormalities, including joint stiffness and abnormal curvature of the spine, are common in affected individuals.

Due to the rarity of Levy-Yeboa Syndrome, there is limited information available regarding its long-term prognosis and treatment options. However, early intervention and supportive therapies can help manage the symptoms and improve the quality of life for individuals with this condition.