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Journal of Child Neurology
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Craniodigital Syndrome of Scott: Clinical and Neuroradiological Features of a New Case

Donatella Milani, MD

Paediatric Department, IRCCS Fondazione Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, University of Milan, Italy

Stefano D'Arrigo, MD

Developmental Neurology Department, IRCCS Istituto Neurologico "C. Besta," Milan, Italy

Alessandra Erbetta, MD

Department of Neuroradiology, IRCCS Istituto Neurologico "C. Besta, Milan, Italy

Angelo Selicorni, MD

Paediatric Department, IRCCS Fondazione Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, University of Milan, Italy

Daria Riva, MD

Developmental Neurology Department, IRCCS Istituto Neurologico "C. Besta," Milan, Italy

Chiara Pantaleoni, MD

Developmental Neurology Department, IRCCS Istituto Neurologico "C. Besta," Milan, Italy, pantaleoni{at}istituto-besta.it

We report on a girl presenting with mental retardation, craniofacial dysmorphisms, and syndactyly. The child's mother and maternal grandfather presented bilateral syndactyly of toes 2 and 3. These manifestations, falling within the ambit of what has been termed the craniodigital syndromes, were first reported by Scott et al (1971) in 3 brothers.

Key Words: craniodigital syndrome • syndactyly • Chiari I

Journal of Child Neurology, Vol. 22, No. 7, 883-886 (2007)
DOI: 10.1177/0883073807304195
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