Acrocallosal syndrome: report of five Turkish patients

Gul D., Ulucan H., Unay B., Akin R., Gokcay E.

CLINICAL DYSMORPHOLOGY, vol.13, no.4, pp.241-246, 2004 (SCI-Expanded) identifier identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 13 Issue: 4
  • Publication Date: 2004
  • Doi Number: 10.1097/00019605-200410000-00008
  • Journal Name: CLINICAL DYSMORPHOLOGY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.241-246
  • Istanbul University Affiliated: No

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. (C) 2004 Lippincott Williams Wilkins.