Heterotopias

dc.contributor.authorKundu, Mrinmoy
dc.contributor.authorAwuah, Wireko Andrew
dc.contributor.authorNg, Jyi Cheng
dc.contributor.authorHuang, Helen
dc.contributor.authorNazir, Abubakar
dc.contributor.authorTabassum, Shehroze
dc.contributor.authorJiffry, Riaz
dc.date.accessioned2025-05-10T15:21:42Z
dc.date.issued2014
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractGMH is a rather common condition of neuronal migration disorders. GMH is associated with seizures and epilepsy, and may cause intellectual disabilities and developmental delay, causing a huge impact on normal childhood development. Even though previous studies have identified genetic and epigenetic risk factors associated with the development of GMH, the actual mechanism causing GMH remains unclear. The severity of the clinical presentation and prognosis of GMH depends on the type, size, and location. Therefore, defining the type and extent of GMH is useful in outlining the management and predicting patients’ prognosis and outcome. © The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG 2024.
dc.identifier.doi10.1007/9783031586309_16
dc.identifier.endpage208
dc.identifier.isbn978-303158630-9
dc.identifier.isbn978-303158629-3
dc.identifier.scopus2-s2.0-85206132142
dc.identifier.scopusqualityN/A
dc.identifier.startpage193
dc.identifier.urihttps://doi.org/10.1007/9783031586309_16
dc.identifier.urihttps://hdl.handle.net/20.500.14730/6129
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherSpringer Nature
dc.relation.ispartofCongenital Brain Malformations: Clinical and Surgical Aspects
dc.relation.publicationcategoryKitap Bölümü - Uluslararası
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20250302
dc.titleHeterotopias
dc.typeBook Part

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