Apert's Syndrome
- 1 March 1969
- journal article
- case report
- Published by Taylor & Francis in Postgraduate Medicine
- Vol. 45 (3) , 158-162
- https://doi.org/10.1080/00325481.1969.11697059
Abstract
Apert's syndrome is a rare condition characterized by a tetrad of features: acrocephaly, facial deformities, ocular proptosis with visual defect, and syndactyly. The patient in the case described is a 13 year old girl without a family history of similar anomalies.Keywords
This publication has 4 references indexed in Scilit:
- PROGRESSIVE SYNOSTEOSIS IN APERT'S SYNDROME (ACROCEPHALOSYNDACTYLY)American Journal of Roentgenology, 1966
- Apert's AcrocephalosyndactylismRadiology, 1962
- Acrocephalosyndactyly with report of a caseThe British Journal of Radiology, 1953
- Acrocephalosyndactyly a Case with Congenital Cardiac AbnormalitiesThe British Journal of Radiology, 1952