Tarani Luigi, Del Balzo Francesca, Costantino Francesco, Properzi Enrico, D'Eufemia Patrizia, Liberati Natascia, Spalice Alberto
Chair of Paediatrics, Department of Paediatrics, University "La Sapienza", Rome, Italy.
Pediatr Rep. 2010 Jun 18;2(1):e8. doi: 10.4081/pr.2010.e8.
Chiari type I malformation (CMI) is a congenital hindbrain anomaly characterized by downward displacement of the cerebellar tonsils through the foramen magnum. Chiari type I malformation often presents with a complex clinical picture and can be sporadic or linked to a variety of genetic conditions. We report on a girl in whom Chiari type I malformation was associated with hypoglycemia, headache, vertigo, syncope and hepatic steatosis. We hypothesize that these symptoms are primarily a consequence of Chiari type I malformation.
Chiari I型畸形(CMI)是一种先天性后脑异常,其特征是小脑扁桃体通过枕骨大孔向下移位。Chiari I型畸形常表现出复杂的临床症状,可为散发性或与多种遗传疾病相关。我们报告了一名患有Chiari I型畸形并伴有低血糖、头痛、眩晕、晕厥和肝脂肪变性的女孩。我们推测这些症状主要是Chiari I型畸形的结果。