The central nervous system in the Apert syndrome

M. M. Cohen, S. Kreiborg

Research output: Contribution to journalArticlepeer-review

161 Citations (Scopus)

Abstract

In this paper, we present available central nervous system data from our series of patients with the Apert syndrome. Combining our own data with that available in the literature, 30 patients had malformations of the corpus callosum, the limbic structures, or both. Other frequent findings included megalencephaly (7 cases), gyral abnormalities (8 cases), encephalocele (4 cases), pyramidal tract abnormalities (2 cases), hypoplasia of cerebral white matter (4 cases), and heterotopic gray matter (2 cases). Progressive hydrocephalus seems to be uncommon and has frequently been confused with nonprogressive ventriculomegaly in the past. Psychometric evaluations, neurological findings, and neuropathologic reports from the literature are critically reviewed. It is clear that a significant number of patients with the Apert syndrome are mentally retarded. It is suggested that malformations of the central nervous system may be responsible for most cases.

Original languageEnglish
Pages (from-to)36-45
Number of pages10
JournalAmerican Journal of Medical Genetics
Volume35
Issue number1
DOIs
Publication statusPublished - 1990

ASJC Scopus Subject Areas

  • Genetics(clinical)

PubMed: MeSH publication types

  • Journal Article
  • Review

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