Moebius Syndrome Overview
Learn About Moebius Syndrome
Moebius syndrome is a rare neurological condition that primarily affects the muscles that control facial expression and eye movement. The signs and symptoms of this condition are present from birth.
The causes of Moebius syndrome are unknown, although the condition probably results from a combination of environmental and genetic factors. Researchers are working to identify and describe specific genes related to this condition. The disorder appears to be associated with changes in particular regions of chromosomes 3, 10, or 13 in some families. Certain medications taken during pregnancy and abuse of drugs such as cocaine may also be risk factors for Moebius syndrome.
The exact incidence of Moebius syndrome is unknown. Researchers estimate that the condition affects 1 in 50,000 to 1 in 500,000 newborns.
Most cases of Moebius syndrome are sporadic, which means they occur in people with no history of the disorder in their family. A small percentage of all cases have been reported to run in families; however, the condition does not have a single clear pattern of inheritance.
Bernardo Bianchi practices in Genoa, Italy. Mr. Bianchi is rated as an Elite expert by MediFind in the treatment of Moebius Syndrome. His top areas of expertise are Facial Paralysis, Charlie M Syndrome, Moebius Syndrome, Osteotomy, and Endovascular Embolization.
Darren Oystreck practices in Stellenbosch, South Africa. Mr. Oystreck is rated as an Elite expert by MediFind in the treatment of Moebius Syndrome. His top areas of expertise are Moebius Syndrome, Charlie M Syndrome, Duane-Radial Ray Syndrome, and Brown Syndrome.
University Medical Associates Of The Medical University Of South Carol
Scott Benjamin is a Physiatrist in Charleston, South Carolina. Dr. Benjamin is rated as an Advanced provider by MediFind in the treatment of Moebius Syndrome. His top areas of expertise are Hemiplegia, Cerebral Palsy, Spastic Diplegia Infantile Type, and Alternating Hemiplegia of Childhood. Dr. Benjamin is currently accepting new patients.
Summary: The purpose of this study is to identify genes associated with impaired development and function of the cranial nerves and brainstem, which may result in misalignment of the eyes (strabismus) and related conditions.
Published Date: April 01, 2016
Published By: National Institutes of Health