3 Search Results for: CLN5
NORD Rare Disease Database
Juvenile CLN3 Disease
Summary Juvenile CLN3 disease, a rare genetic disorder, belongs to a group of progressive degenerative neurometabolic disorders known as the neuronal ceroid...
Also known as: CLN3, CLN3-NCL, JNCL, juvenile Batten disease, juvenile neuronal ceroid lipofuscinosis , neuronal ceroid lipofuscinosis 3, Spielmeyer-Sjogren disease, Vogt-Spielmeyer disease, Vogt-Spielmeyer-Sjogren disease
Adult Neuronal Ceroid Lipofuscinosis
Summary Adult neuronal ceroid lipofuscinosis (ANCL) is a general term for several rare genetic disorders that belong to a group of progressive, degenerative...
Also known as: adult NCL, ANCL, Kufs syndrome, Kufs disease, Parry disease, neuronal ceroid lipofuscinosis, adult type
NIH GARD Information
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 5 (CLN5-NCL) is a rare condition that affects the nervous system. Signs and symptoms of the condition generally develop between ages 4.5...
