Center for Chronically Sick Children, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Center for Chronically Sick Children, Charité - Universitätsmedizin Berlin, Berlin, Germany; Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Pediatr Neurol. 2020 Nov;112:47-52. doi: 10.1016/j.pediatrneurol.2020.07.013. Epub 2020 Aug 11.
Agenesis of the corpus callosum is a rare congenital brain malformation that can be associated with other cerebral malformations and/or underlying genetic causes. Prenatal counseling is hampered due to the lack of reliable long-term data on neurodevelopmental outcome.
Since 2010, a total of 23 children with agenesis of the corpus callosum (mean age 3.8 years, range 0.7 to 9.7 years) were registered in our ACC outpatient clinic and diagnosed in a standardized manner; the data were analyzed retrospectively. Prenatal and postnatal imaging, associated malformations, genetic and clinical findings, and psychological testing (Bayley Scales, Kaufman Assessment Battery for Children II, Snijders-Oomen Non-verbal Test, Wechsler Preschool and Primary Scale I-III) were included. The clinical outcome was classified as "normal" (intelligence quotient 85 to 115, unremarkable motor skills), "moderate developmental delay" (intelligence quotient 70 to 85, mild motor abnormalities), and "severe developmental delay" (intelligence quotient less than 70, severe movement disorder).
Isolated corpus callosum malformation was diagnosed in 15 of 23 (65%), associated cerebral malformations in four of 23 (17%), and associated cerebral malformations plus intracranial cyst in four of 23 (17%) children. Prenatal diagnosis changed in nine of 23 (39%) cases. Overall, a normal outcome or moderate or severe developmental delay was present in 15 of 23 (65%) or five of 23 (22%) or three of 23 (13%) children, respectively. Also six of eight children with associated cerebral malformations showed normal outcome.
Our findings support the notion that developmental outcome is favorable in about two-thirds of children with prenatally diagnosed agenesis of corpus callosum. However, the individual outcome in children with agenesis of corpus callosum is difficult to predict. Even children with correctly characterized phenotypes show a variety of outcomes, making prenatal counseling challenging.
胼胝体发育不全是一种罕见的先天性脑畸形,可伴有其他脑畸形和/或潜在的遗传原因。由于缺乏关于神经发育结果的可靠长期数据,产前咨询受到阻碍。
自 2010 年以来,共有 23 例胼胝体发育不全的儿童(平均年龄 3.8 岁,范围 0.7 至 9.7 岁)在我们的 ACC 门诊注册,并以标准化方式进行诊断;数据进行回顾性分析。包括产前和产后影像学、相关畸形、遗传和临床发现以及心理测试(贝利量表、考夫曼儿童评估量表第二版、斯内德斯-奥曼非言语测试、韦氏学前和小学量表 I-III)。临床结果分为“正常”(智商 85 至 115,运动技能无异常)、“中度发育迟缓”(智商 70 至 85,轻度运动异常)和“重度发育迟缓”(智商低于 70,严重运动障碍)。
23 例中有 15 例(65%)诊断为单纯胼胝体畸形,23 例中有 4 例(17%)诊断为相关脑畸形,23 例中有 4 例(17%)诊断为相关脑畸形伴颅内囊肿。23 例中有 9 例(39%)产前诊断发生变化。总的来说,15 例(65%)或 5 例(22%)或 3 例(13%)儿童的结果为正常或中度或重度发育迟缓。此外,8 例伴有脑畸形的儿童中有 6 例结果正常。
我们的研究结果支持这样一种观点,即大约三分之二的产前诊断为胼胝体发育不全的儿童发育结果良好。然而,胼胝体发育不全儿童的个体预后难以预测。即使是具有明确特征表型的儿童,也表现出多种结果,使产前咨询具有挑战性。