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- A Tiwari, A Agrawal, A Pratap, R Lakshmi, and R Narad.
- Department of Radiology, B P Koirala Institute of Health Sciences, Dharan, Nepal.
- Singap Med J. 2007 Feb 1; 48 (2): e62-5.
AbstractApert syndrome is characterised by craniosynostosis, associated with maxillary hypoplasia, symmetrical syndactyly of the hands and feet, and other systemic malformations including mental retardation. Apert syndrome and septo-optic dysplasia is rarely described. We describe the classical clinical and radiological findings of this syndrome in a 20-year-old woman. Though early surgical intervention is imperative for optimal outcome, in developing countries, it may not be possible to intervene at the right time due to financial constraints.
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