Parkinson disease 3, autosomal dominant

Parkinson disease 3, autosomal dominant is a rare form of Parkinson disease that is inherited in an autosomal dominant pattern. Although detailed definitions are not currently available, this condition is known to be linked to genetic changes in the PARK3 gene. Research on this condition has been limited, and available information has been obtained from sources such as the Online Mendelian Inheritance in Man (OMIM) and the Genetic and Rare Diseases Information Center (GARD). More detailed descriptions of how this condition affects people and its natural history are still under review.

Information about symptoms is currently limited for this condition.

This condition is inherited in an autosomal dominant manner. Changes in the PARK3 gene are identified as a cause. The genetic basis of the disease means that a family history may be present in people with this condition.

Information about treatment options is currently limited for this condition.

Information about prognosis and quality of life is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.