Cerebelloparenchymal Disorder 3


Type of disease: Rare conditions

Cerebelloparenchymal Disorder 3 is a rare inherited disorder characterized by albinism (pale-white skin color), incoordination, low muscle tone, and eye abnormalities. Symptoms include: abnormal walking pattern, weakness, poor coordination (ataxia), and retinal albinism, which may affect vision. This condition has been reported in a few families, and is autosomal recessive, meaning that it is only sometimes passed from parents to their children. Treatment varies on a case-by-case basis, and may include therapies such as speech therapy.

Connect. Empower. Inspire.