Chiari I malformation: Case report

Authors

  • Dhiego Alves de Lacerda
  • Pedro Fechine Honorato
  • Anna Vitória Paz Moreira
  • Isabelle Lima Lustosa
  • Renata Silva Cezar
  • Pedro Lima Leite
  • Bianca Caldeira Leite
  • Jalles Dantas de Lucena
  • Anaylle Vieira Lacerda de  Oliveira

Keywords:

Chiari I malformation, Clinical implications, Case report

Abstract

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).

 

DOI:https://doi.org/10.56238/sevenIVmulti2023-159

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Published

2023-12-20

How to Cite

Lacerda, D. A. de, Honorato, P. F., Moreira, A. V. P., Lustosa, I. L., Cezar, R. S., Leite, P. L., Leite, B. C., Lucena, J. D. de, & Oliveira,A.V.L.de . (2023). Chiari I malformation: Case report. Caderno De ANAIS HOME. Retrieved from https://homepublishing.com.br/index.php/cadernodeanais/article/view/1231

Issue

IV SEVEN INTERNATIONAL MULTIDISCIPLINARY CONGRESS

Section

Articles