Acrocallosal syndrome: report of five Turkish patients

Acrocallosal syndrome is characterized by agenesis of the corpus callosum, craniofacial anomalies, psychomotor retardation, and polydactyly. The clinical spectrum of this syndrome is broader than previous reports suggest. Five Turkish patients including dizygotic twins are reported.

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Bibliographic Details
Published in:	Clinical dysmorphology Vol. 13; no. 4; pp. 241 - 246
Main Authors:	Gül, Davut, Ulucan, Hakan, Ünay, Bülent, Akın, Rıdvan, Gökçay, Erdal
Format:	Journal Article
Language:	English
Published:	England Wolters Kluwer Health, Inc. All rights reserved 01-10-2004
Subjects:	Agenesis of Corpus Callosum Child Child, Preschool Corpus Callosum - diagnostic imaging Craniofacial Abnormalities - physiopathology Female Humans Infant Magnetic Resonance Spectroscopy Male Polydactyly - physiopathology Psychomotor Disorders - physiopathology Radiography Syndrome Turkey
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Description
Summary:	Acrocallosal syndrome is characterized by agenesis of the corpus callosum, craniofacial anomalies, psychomotor retardation, and polydactyly. The clinical spectrum of this syndrome is broader than previous reports suggest. Five Turkish patients including dizygotic twins are reported.
Bibliography:	ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3
ISSN:	0962-8827
DOI:	10.1097/00019605-200410000-00008