3 Search Results for: CLN1
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
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
Ceroid lipofuscinosis neuronal 1
