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Acrocallosal syndrome: report of five Turkish patients
Davut Gül1, Hakan Ulucan, Bülent Ünay
1Department of Medical Genetics, GATA Medical School, Ankara, Turkey Department of Medical Genetics Adnan Menderes University School of Medicine, Aydin, Turkey Department of Pediatric Neurology, GATA Medical School, Ankara, Turkey.
Clinical Dysmorphology
|September 15, 2004
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.