What is another word for Spielmeyer-vogt Disease?
Pronunciation: [spˈiːlma͡ɪ͡əvˈɒɡt dɪzˈiːz] (IPA) 
Spielmeyer-Vogt disease, also known as neuronal ceroid lipofuscinosis type 3 (NCL3), is a rare genetic disorder that causes a progressive deterioration of the nervous system. This condition is characterized by the accumulation of lipopigments in the brain and nervous system tissues, leading to a loss of vision, motor skills, and cognitive function. There are no known cures for Spielmeyer-Vogt disease, and treatment is focused on managing symptoms and improving quality of life for patients and their families. Some alternative names for Spielmeyer-Vogt disease include Batten disease, juvenile NCL, and CLN3 disease. These terms are often used interchangeably in medical literature and discussions.
