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  • Title: Acrocallosal syndrome: report of five Turkish patients.
    Author: Gül D, Ulucan H, Ünay B, Akın R, Gökçay E.
    Journal: Clin Dysmorphol; 2004 Oct; 13(4):241-246. PubMed ID: 15365461.
    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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