Chiari I 畸形:病例报告

Dhiego Alves de Lacerda, Pedro Fechine Honorato, Anna Vitória Paz Moreira, Isabelle Lima Lustosa, Renata Silva Cezar, Pedro Leite Neto, Anaylle Vieira Lacerda de Oliveira, Bianca Caldeira Leite, Marineide Domingos da Silva, Jalles Dantas de Lucena
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引用次数: 0

摘要

阿诺德-奇拉氏 I 型畸形(CM-I)是一种遗传疾病,由汉斯-奇拉氏(Hans Chiari)于 1891 年首次描述(SCHIJMAN,2004 年)。CM-I 的特征是小脑扁桃体从枕骨大孔下缘下降超过 5 毫米,这会阻碍脑脊液(CSF)的流动,并经常与鞘膜积液(BALL;CRONE,1995 年;ROMERO-LUNA 等人,2022 年)联系在一起,由于诊断困难而引起临床神经科的极大关注(MORO 等人,1999 年)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chiari I malformation: Case report
Arnold Chiari type I malformation (CM-I) is a genetic disease first described in 1891 by Hans Chiari (SCHIJMAN, 2004). CM-I is characterized by the descent of the cerebellar tonsils more than 5 mm from the lower margin of the foramen magnum, which can impede the flow of cerebrospinal fluid (CSF) and is often associated with syringomyelia (BALL; CRONE, 1995; ROMERO-LUNA et al., 2022), generating great clinical neurological interest due to the difficulty in diagnosis (MORO et al., 1999).
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