Chiari I malformation: Case report

Autores/as

  • 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

Palabras clave:

Chiari I malformation, Clinical implications, Case report

Resumen

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/sevenIVmulti2023-142

Descargas

Publicado

2023-12-14

Cómo citar

Lacerda, D. A. de, Honorato, P. F., Moreira, A. V. P., Lustosa, I. L., Cezar, R. S., Neto, P. L., Oliveira,A.V.L.de , Leite, B. C., Silva, M. D. da, & Lucena, J. D. de. (2023). Chiari I malformation: Case report. Caderno De ANAIS HOME. Recuperado a partir de https://homepublishing.com.br/index.php/cadernodeanais/article/view/1214

Número

IV SEVEN INTERNATIONAL MULTIDISCIPLINARY CONGRESS

Sección

Articles