RELATED: Tipp City family raising awareness of rare disease affecting 7-year-old boy Grayson Naff is living with Neuronal Ceroid Lipofuscinosis, otherwise known as Batten disease, a rare genetic ...

eye problems (including collie eye anomaly), neuronal ceroid lipofuscinosis and trapped neutrophil syndrome. Good breeders will provide prospective owners with a puppy’s parents’ screening ...

Polaryx Therapeutics is working to bring patient-friendly treatments to people with ultra-rare genetic disorders known as neuronal ceroid lipofuscinoses (NCLs), the most common of which is Batten ...

The company will use the funds to advance gene therapies for CNS disorders such as neuronal ceroid lipofuscinosis type 2 and Huntington's disease.

eye problems (including collie eye anomaly), neuronal ceroid lipofuscinosis and trapped neutrophil syndrome. Good breeders will provide prospective owners with a puppy's parents' screening tests ...

In recent years, advances in molecular genetics have impacted the understanding and the classification of hereditary retinal and optic nerve disease perhaps more than any other group of eye ...

Neuronal ceroid lipofuscinosis type 2 (CLN2) is a very rare inherited condition affecting between 3 and 6 babies each year in the UK. It’s a progressive condition, also known as Batten disease, and ...

Although apoptosis has not been previously studied in EPM1, neuronal apoptotic cell death has been found in the related PME Batten disease 47 (juvenile neuronal ceroid lipofuscinosis, JNCL).

J Child Neurol. 2004;19(8):571-578. Patients with an isolated visually induced seizure in special circumstances, with or without a photoparoxysmal response on the EEG. This group comprises ...

Juvenile Batten disease belongs to a group of disorders referred to as neuronal ceroid lipofuscinoses (NCLs). Over 400 different errors in 13 genes have been attributed to various forms of NCL ...