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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Veröffentlicht in:Clinical dysmorphology 2004-10, Vol.13 (4), p.241-246
Hauptverfasser: Gül, Davut, Ulucan, Hakan, Ünay, Bülent, Akın, Rıdvan, Gökçay, Erdal
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Sprache:eng
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Zusammenfassung: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.
ISSN:0962-8827
DOI:10.1097/00019605-200410000-00008