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Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene
Congenital hydrocephalus is considered as either acquired due to haemorrhage, infection or neoplasia or as of developmental nature and is divided into two subgroups, communicating and obstructive. Congenital hydrocephalus is either syndromic or non-syndromic, and in the latter no cause is found in m...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Acta Neuropathol Commun |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5412059/ https://ncbi.nlm.nih.gov/pubmed/28460636 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-017-0438-4 |
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