Acrocallosal syndrome: report of five Turkish patients


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

CLINICAL DYSMORPHOLOGY, cilt.13, ss.241-246, 2004 (SCI İndekslerine Giren Dergi) identifier identifier identifier identifier

  • Cilt numarası: 13 Konu: 4
  • Basım Tarihi: 2004
  • Doi Numarası: 10.1097/00019605-200410000-00008
  • Dergi Adı: CLINICAL DYSMORPHOLOGY
  • Sayfa Sayıları: ss.241-246

Özet

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.