Demographic, ocular and associated neurological findings in corpus callosum malformations

BİNGÖL KIZILTUNÇ P., ŞAHLI E., Idil A., ATİLLA H.

TURKISH JOURNAL OF PEDIATRICS, cilt.63, sa.2, ss.291-299, 2021 (SCI-Expanded) identifier identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 63 Sayı: 2
  • Basım Tarihi: 2021
  • Doi Numarası: 10.24953/turkjped.2021.02.013
  • Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, CAB Abstracts, EMBASE, MEDLINE, Veterinary Science Database, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.291-299
  • Anahtar Kelimeler: agenesis, corpus callosum, hypoplasia, low vision, magnetic resonance imaging, MULTIPLE-SCLEROSIS, AGENESIS, DIAGNOSIS, ATROPHY
  • Ankara Üniversitesi Adresli: Evet

Özet

Background. The corpus callosum is a primary commissural part of the brain which connects the two hemispheres. Processing sensory, motor, visuo-motor and cognitive functions are related to a healthy connection. In this study, we aimed to evaluate the ocular, neurologic and other systemic findings of corpus callosum malformations and to focus on the association between the ocular and neurological findings and the type of callosal malformation according to cranial magnetic resonance imaging (MRI).