Acrocallosal syndrome: Report of five Turkish patients
Clinical Dysmorphology, cilt.13, sa.4, ss.241-246, 2004 (Scopus)
- 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: Scopus
- Sayfa Sayıları: ss.241-246
- Anahtar Kelimeler: Acrocallosal, Autosomal recessive, Corpus callosum, Leucomalacia, Mental retardation, Polydactyly
- Sağlık Bilimleri 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 sugges. Five Turkish patients including dizygotic twins are reported. © 2004 Lippincott Williams & Wilkins.