User:CH388 Team5

Introduction
Kufor-Rakeb syndrome is an autosomal recessive disease. It is a form of juvenile-onset atypical Parkinson disease (PARK9). The OMIM number is 606693. It was identified to be associated with chromosome 1p36, which was assigned PARK9.

ATP13A2 gene mutations are associated with Kufor-Rakeb syndrome. Patients have been identified to have iron in their basal ganglia.

Signs and Symptoms
signs and symptoms