1. An analysis of 109 fetuses with prenatal diagnosis of complete agenesis of corpus callosum
- Author
-
Selim Doganay, Mehmet Canpolat, Mustafa Basbug, Mahmut Tuncay Ozgun, Hakan Gümüş, Hüseyin Per, Ayşe Kaçar Bayram, Mehmet Serdar Kutuk, and Sefer Kumandaş
- Subjects
Heart Defects, Congenital ,Male ,Pediatrics ,medicine.medical_specialty ,Neurology ,Developmental Disabilities ,Prenatal diagnosis ,Dermatology ,Corpus callosum ,behavioral disciplines and activities ,Congenital Abnormalities ,03 medical and health sciences ,0302 clinical medicine ,Pregnancy ,Intellectual Disability ,Prenatal Diagnosis ,Medicine ,Humans ,030212 general & internal medicine ,Agenesis of the corpus callosum ,Child ,Cause of death ,Retrospective Studies ,business.industry ,Incidence (epidemiology) ,Infant, Newborn ,General Medicine ,medicine.disease ,Magnetic Resonance Imaging ,Psychiatry and Mental health ,stomatognathic diseases ,Fetal Diseases ,Respiratory failure ,nervous system ,Agenesis ,Female ,Neurology (clinical) ,Agenesis of Corpus Callosum ,business ,Respiratory Insufficiency ,human activities ,030217 neurology & neurosurgery ,psychological phenomena and processes - Abstract
Background Agenesis of the corpus callosum (ACC) is the most frequent commissural malformation of the brain. It continues to be an important cause of the pregnancy termination associated with the central nervous system (CNS). Objective The aim of the study is to provide a comprehensive assessment of fetuses with diagnosis of complete ACC, as well as postnatal neurodevelopmental outcomes. Methods The data of 75,843 fetuses were screened for evaluation of complete ACC between 2003 and 2017, and a total of 109 cases with complete ACC were included in the study. ACC was considered isolated when no additional anomalies were detected, and ACC was considered complex when additional anomalies were present. Results The prevalence of complete ACC was 9.4 per 10,000 live births, and the incidence was ranged from 1.8 to 16.6 per 10,000 person-years. Patients with isolated ACC had a significantly higher survival when compared with patients with complex ACC (97.4%, n = 38/39 vs. 68.8%, n = 22/32, P = 0.001).The most important cause of death were congenital heart disease and/or respiratory failure during neonatal period. Developmental and intellectual disabilities were significantly higher in the complex ACC cases (P < 0.001). Postnatal neurodevelopmental outcomes were completely normal in 79.4% of cases with isolated ACC. Conclusions Isolated complete ACC is usually associated with a favorable outcome. The most important prognostic factors are the presence or absence of associated congenital anomalies.
- Published
- 2019