Craniodigital Syndrome of Scott: Clinical and Neuroradiological Features of a New Case-Reference-Cited by-同舟云学术

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

Published:2007-07 Issue:7 Volume:22 Page:883-886
ISSN:0883-0738
Container-title:Journal of Child Neurology
language:en
Short-container-title:J Child Neurol

Author:

Milani Donatella¹,D'Arrigo Stefano²,Erbetta Alessandra³,Selicorni Angelo¹,Riva Daria²,Pantaleoni Chiara⁴

Affiliation:

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

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

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

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

Abstract

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.

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/0883073807304195

Reference5 articles.

1. The craniodigital syndrome of Scott: Report of a second family

2. A new craniodigital syndrome with mental retardation

3. Practice parameter: Evaluation of the child with global developmental delay [RETIRED]

4. Craniodigital syndromes: Report of a child with Filippi syndrome and discussion of differential diagnosis

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