Cargando…
Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants
The prevalence of congenital hydrocephalus has been estimated at 1.1 per 1000 infants when including cases diagnosed before 1 year of age after exclusion of neural tube defects. Classification criteria are based either on CSF dynamics, pathophysiological mechanisms or associated lesions. Whereas inh...
Autores principales: | Marguet, Florent, Vezain, Myriam, Marcorelles, Pascale, Audebert-Bellanger, Séverine, Cassinari, Kévin, Drouot, Nathalie, Chambon, Pascal, Gonzalez, Bruno J., Horowitz, Arie, Laquerriere, Annie, Saugier-Veber, Pascale |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183048/ https://www.ncbi.nlm.nih.gov/pubmed/34092257 http://dx.doi.org/10.1186/s40478-021-01207-5 |
Ejemplares similares
-
Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly
por: Friocourt, Gaëlle, et al.
Publicado: (2010) -
Inference of Diagnostic Markers and Therapeutic Targets From CSF Proteomics for the Treatment of Hydrocephalus
por: Horowitz, Arie, et al.
Publicado: (2020) -
Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene
por: Saugier-Veber, Pascale, et al.
Publicado: (2017) -
Murine MPDZ‐linked hydrocephalus is caused by hyperpermeability of the choroid plexus
por: Yang, Junning, et al.
Publicado: (2018) -
Prenatal alcohol exposure is a leading cause of interneuronopathy in humans
por: Marguet, Florent, et al.
Publicado: (2020)