Classification, diagnosis and potential mechanisms in Pontocerebellar Hypoplasia

Pontocerebellar Hypoplasia (PCH) is group of very rare, inherited progressive neurodegenerative disorders with prenatal onset. Up to now seven different subtypes have been reported (PCH1-7). The incidence of each subtype is unknown. All subtypes share common characteristics, including hypoplasia/atr...

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Detalles Bibliográficos
Autores principales: Namavar, Yasmin, Barth, Peter G, Poll-The, Bwee Tien, Baas, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159098/
https://www.ncbi.nlm.nih.gov/pubmed/21749694
http://dx.doi.org/10.1186/1750-1172-6-50

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159098/
https://www.ncbi.nlm.nih.gov/pubmed/21749694
http://dx.doi.org/10.1186/1750-1172-6-50

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