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Rare Disease Database

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...