| Literature DB >> 3960322 |
L A Alvarez, T Yamamoto, B Wong, T J Resnick, J F Llena, S L Moshé.
Abstract
A patient with the typical craniofacial features and clinical course of Miller-Dieker syndrome (MDS) was found on autopsy to have focal pachygyria rather than lissencephaly. The brainstem and cerebellum were hypoplastic, but thalami and basal ganglia were normal. We believe that MDS is a syndrome in which multiple specific pathways of neuronal migration are affected selectively, such as migration to the neocortex, migration via corpus pontobulbare, and cerebellar migration. However, another migration pathway (via corpus gangliothalamicum) is spared.Entities:
Mesh:
Year: 1986 PMID: 3960322 DOI: 10.1212/wnl.36.4.489
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910