Acrocallosal syndrome: report of five Turkish patients

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

CLINICAL DYSMORPHOLOGY, cilt.13, sa.4, ss.241-246, 2004 (SCI-Expanded) identifier identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 13 Sayı: 4
  • Basım Tarihi: 2004
  • Doi Numarası: 10.1097/00019605-200410000-00008
  • Dergi Adı: CLINICAL DYSMORPHOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.241-246
  • İstanbul Üniversitesi Adresli: Hayır

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.