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Rare Disease Database

5 Search Results for: CLN3


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

Classic Infantile CLN1 Disease

Summary Classic infantile CLN1 disease is a rare genetic disorder with an onset of symptoms between 6 and 24 months of age. CLN1 disease is characterized by delays in...

Also known as: CLN1, INCL, Infantile Finnish type neuronal ceroid lipofuscinosis (Balkan disease), Infantile NCL, Infantile neuronal ceroid lipofuscinosis, Santavuori-Haltia Disease, Santavuori disease

NIH GARD Information

Neuronal ceroid lipofuscinosis 10

Neuronal ceroid lipofuscinosis 10 (CLN10 disease) is a type of neuronal ceroid lipofuscinosis (NCL), a group of severe diseases that affect the nervous...

Neuronal ceroid lipofuscinosis 3

Neuronal ceroid lipofuscinosis 3 (CLN3-NCL) is a rare condition that affects the nervous system. Signs and symptoms generally develop between age 4 and 8 years, although...