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[Crouzon's disease with papillary stasis]
1Clinica Oftalmologică, Craiova.
Oftalmologia (Bucharest, Romania : 1990)
|July 1, 1993
Summary
This case study highlights Crouzon syndrome in a 3-year-old, presenting with prominent forehead, eye issues, and developmental delays. Early diagnosis of this rare craniofacial disorder is crucial for management.
Area of Science:
- Pediatric Neurology
- Clinical Genetics
- Craniofacial Surgery
Background:
- Crouzon syndrome is a genetic disorder characterized by premature fusion of skull bones.
- It leads to distinctive facial features and potential neurological complications.
- Autosomal dominant inheritance with high penetrance is typical.