Neuronal ceroid lipofuscinosis type 2: an Australian case series

AIM: Late infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease is a rare neurodegenerative disorder presenting in children aged 2–4 years with seizures and loss of motor and language skills, followed by blindness and death in late childhood. Initial presenting features are similar to a ran...

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Detalles Bibliográficos
Autores principales: Johnson, Alexandra M, Mandelstam, Simone, Andrews, Ian, Boysen, Katja, Yaplito‐Lee, Joy, Fietz, Michael, Nagarajan, Lakshmi, Rodriguez‐Casero, Victoria, Ryan, Monique M, Smith, Nicholas, Scheffer, Ingrid E, Ellaway, Carolyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497200/
https://www.ncbi.nlm.nih.gov/pubmed/32329550
http://dx.doi.org/10.1111/jpc.14890

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497200/
https://www.ncbi.nlm.nih.gov/pubmed/32329550
http://dx.doi.org/10.1111/jpc.14890

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