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.
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References
Apert ME (1906) L'acrocéphalosyndactylie. Bull Med Soc Hop Paris 23: 13310–13330
Blank CE (1960) Apert's syndrome: observations on a British series of 39 cases. Humangenetik 24: 151–164
David JD, Poswillo D, Simpson D (1982) The craniosynostoses. Springer, Berlin Heidelberg New York, p 5
Hogan GR, Bauman ML (1971) Hydrocephalus in Apert's syndrome. J Paediatr 79: 782–787
Humphreys RP (1991) Diagnosis and treatment of craniosynostosis and intra-cranial anomalies. Clin Plast Surg 18: 231–235
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Hanieh, A., David, D.J. Apert's syndrome. Child's Nerv Syst 9, 289–291 (1993). https://doi.org/10.1007/BF00306277
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DOI: https://doi.org/10.1007/BF00306277