A unique association of Marfan syndrome with craniofacial hypoplasia, oligophrenia and severe microphthalmia
- PMID: 3220717
- DOI: 10.1007/BF02334006
A unique association of Marfan syndrome with craniofacial hypoplasia, oligophrenia and severe microphthalmia
Abstract
The present report describes a case of Marfan syndrome with microphthalmia, facial and cerebral hemiatrophy and oligophrenia. This association has never previously been described in patients with Marfan disease.
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