Brill C B, Gutierrez J, Mishkin M M
Department of Pediatrics, Thomas Jefferson University Hospital, Philadelphia, PA, USA.
J Child Neurol. 1997 Feb;12(2):101-6. doi: 10.1177/088307389701200206.
Chiari I malformation, a congenital abnormality in which deformed cerebellar tonsils are displaced downward through the foramen magnum, commonly presents in patients with headache or symptoms of dysfunction of the cerebellum, brain stem, and cervical spinal cord. We report 11 children with Chiari I malformation who presented with seizures and developmental delay in motor or language function with or without autistic features. To our knowledge, an association between Chiari I malformation and seizures or neurodevelopmental deficits or both has not been previously reported. We believe that Chiari I malformation should not be considered an incidental finding in these patients, but may be a marker for subtle cerebral dysgenesis. Chiari I and II malformations may constitute a complex but continuous spectrum, related to the timing and severity of a shared underlying embryologic mechanism.
Chiari I畸形是一种先天性异常,表现为畸形的小脑扁桃体通过枕骨大孔向下移位,常见于有头痛或小脑、脑干及颈脊髓功能障碍症状的患者。我们报告了11例患有Chiari I畸形的儿童,他们出现了癫痫发作以及运动或语言功能发育迟缓,伴有或不伴有自闭症特征。据我们所知,此前尚未报道过Chiari I畸形与癫痫发作或神经发育缺陷或两者之间的关联。我们认为,在这些患者中,Chiari I畸形不应被视为偶然发现,而可能是细微脑发育异常的一个标志。Chiari I型和II型畸形可能构成一个复杂但连续的谱系,与共同潜在胚胎学机制的时间和严重程度相关。