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Acrocallosal syndrome: report of five Turkish patients
Authors:Gül Davut  Ulucan Hakan  Unay Bülent  Akin Ridvan  Gökçay Erdal
Affiliation:Department of Medical Genetics, GATA Medical School, Ankara, Turkey. davutgul2001@yahoo.com
Abstract:
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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