Jackson-Weiss Syndrome (JWS) is a rare genetic disorder characterized by foot abnormalities. Symptoms include abnormally broad big toes, webbing of the skin between the second and third toes, an inward angling of the toes, and/or malformation or fusion of certain bones within the feet. Jackson-Weiss Syndrome is inherited and affects both sexes equally.
Symptoms of Jackson-Weiss syndrome include foot abnormalities, craniosynostosis, and other congenital defects (defects present at birth), including those that cause blindness, seizures, and decreased intellectual capacity.
Typically, the symptoms of Jackson-Weiss syndrome are treated with surgery during the patient's infancy. The surgery is performed in order to: treat the feet or relieve pressure on the brain, provide room in the skull for the brain to grow, and improve the appearance of the head.
If your child is showing symptoms of Jackson-Weiss syndrome, contact your doctor to obtain the help you need. With treatment from an experienced doctor, many patients with the syndrome are able to lead healthy, happy lives.
If you have any symptoms, call us at Southeast Podiatry to make an appointment with Dr. Brent Harwood or Dr. Bradford Egly.