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Published in 2017 at "Acta Neurologica Belgica"
DOI: 10.1007/s13760-017-0871-y
Abstract: Crouzon syndrome (CS) is a rare and complex autosomal dominant craniosynostosis with a highly variable phenotypic appearance and variable penetrance [1]. It was first described by French neurologist Octave Crouzon in 1912 [1]. The genetic…
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Keywords:
epilepsy;
crouzon syndrome;
hypermotor;
sleep ... See more keywords