Synonyms: CLN8 disease, Northern epilepsy variant | NCL, Northern epilepsy variant | Neuronal ceroid lipofuscinosis, Northern epilepsy variant | Northern epilepsy
Progressive epilepsy-intellectual deficit Finnish type (also known as Northern epilepsy) is a subtype of neuronal ceroid lipofuscinosis (NCL; see this term) characterized by seizures progressive decline of intellectual capacities and variable loss of vision.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version September 2024
Newly diagnosed with
Progressive epilepsy-intellectual disability syndrome, Finnish type?
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Advocacy Organizations
DDX3X Foundation
Our mission is to connect families, resources, and the medical community to advance research for a treatment or cure to DDX3X Syndrome. Our ultimate goal is to accelerate brain function in individuals affected by DDX3X Syndrome through advances in cell and gene therapy and pharmaceuticals.
KIF1A.ORG
KIF1A.ORG is a global community dedicated to improving the lives of those affected by KIF1A Associated Neurological Disorder (KAND) and accelerating research to find a cure.
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Clinical Trials
For a list of clinical trials in this disease area, please click here.