Apert's syndrome

A. Hanieh*, D. J. David

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

This paper discusses 33 cases of Apert's syndrome whitc were treated in the Australian Craniofacial unit at the adelaide Children's Hospital. The main features were discussed. We found that mild ventricular dilatation is common in Apert's syndrome but without associated raised intracranial pressure. Severe ventricular dilatation was seen in only one case. No shunt procedures were performed. We also studied the changes in the ventricular size after transcranial corrective procedures. There was no significant change in the ventricular size, the increase in the skull volume was compensated by expansion of the brain tissue and to some extent by increase in the subrachnoid space. Two cases with unusual features are also described.

Original languageEnglish
Pages (from-to)289-291
Number of pages3
JournalChild's Nervous System
Volume9
Issue number5
DOIs
Publication statusPublished - Aug 1993
Externally publishedYes

Keywords

  • Apert's syndrome
  • Calvarial changes
  • Hydrocephalus
  • Intracranial changes
  • Syndactyly

Fingerprint

Dive into the research topics of 'Apert's syndrome'. Together they form a unique fingerprint.

Cite this