Results 91 to 100 of about 21,399,247 (215)

Chiari malformation with concurrent papilledema: a patient-level meta-analysis of case reports and case series

Egyptian Journal of Neurosurgery
Background Chiari I malformation, characterized by the displacement of cerebellar tonsils, and Chiari 1.5, involving cerebellar tonsils and brainstem displacement, share symptoms with Idiopathic Intracranial Hypertension, including headache, paresthesia,
Alejandro Pando, Daniel J. Valdivia, Daniel A. Brenner, Mohammed Ali Alvi, Hai Sun, James K. Liu, Ira Goldstein   +6 more
doaj   +1 more source

Pediatric triad of craniofacial fibrous dysplasia, Chiari malformation type I and syringomyelia: a case report

Acta Neurochirurgica
Fibrous dysplasia is a benign bone disease characterized by the replacement of normal bone tissue with fibrous tissue, resulting in irregular bone structure.
Yaxiong Li, Jianfeng Liu, Jian Guan, Conghui Li   +3 more
doaj   +1 more source

Combined Spinal-Epidural Analgesia for Laboring Parturient with Arnold-Chiari Type I Malformation: A Case Report and a Review of the Literature

Case Reports in Anesthesiology, 2013
Anesthetic management of laboring parturients with Arnold-Chiari type I malformation poses a difficult challenge for the anesthesiologist. The increase in intracranial pressure during uterine contractions, coughing, valsalva maneuvers, and expulsion of ...
Clark K. Choi, Kalpana Tyagaraj
doaj   +1 more source

A less invasive suboccipital decompression-cranioplasty for Chiari type I malformation: Is it beneficial?

Interdisciplinary Neurosurgery, 2018
This was a retrospective study of 10 Chiari Malformation type I patients who were treated by the author since 2010–2016. This study aims to elucidate the benefit of modified foramen magnum decompression by preserving the bone as propose upside down ...
G.B. Mahadewa Tjokorda, G.A. Senapathi Tjokorda   +1 more
doaj   +1 more source

Surgical Management of Chiari Malformation Type I in the Pediatric Patients with Syringomyelia and Related to Klippel-Feil Syndrome: A Case Series and Literature Review

Acta Medica Bulgarica
Chiari type I malformation (CM-1) is a birth defect where the back part of the skull does not develop properly, leading to the formation of a small and shallow space at the back of the head.
Encarnacion-Santos D. A., Chmutin G., Anvardzhonovich I. B., Chmutin E., Arstanbekov B., Kurbonov Sh., Bodanova S., Chaurasia B.   +7 more
doaj   +1 more source

MALFORMAÇÃO DE CHIARI I: RELATO DE CASO

Revista Uningá, 2019
RESUMO Introdução: A Malformação de Chiari tipo I é uma alteração congênita e pouco prevalente que é originária de anomalias estruturais da base do crânio com uma fossa craniana posterior hipoplásica que leva à herniação das tonsilas cerebelares pelo
Illgner Alves de Souza, Matheus Borges Gomes, Guilherme Enares Ramires, Felipe Famelli de Campos, Felipe Iankelevich Baracat   +4 more
doaj  

Rare association between cystic fibrosis, Chiari I malformation, and hydrocephalus in a baby: a case report and review of the literature

Journal of Medical Case Reports, 2011
Introduction Cystic fibrosis, an epithelial cell transport disorder caused by mutations of the cystic fibrosis transmembrane conductance regulator gene, is not generally associated with malformations of the central nervous system.
Jea Andrew, Raol Viraj H, Patel Akash J
doaj   +1 more source

Arachnoiditis and Chiari I malformation [PDF]

Acta Neurochirurgica, 2020
openaire   +2 more sources

Presenting Symptoms of Chiari Type I Malformation

, 2009
Clinical and radiographic predictors of neurologic symptoms were investigated in a population-based retrospective study of 51 children identified with Chiari I malformation at the University of California, and Kaiser Department of Radiology, San ...
J Gordon Millichap
core   +1 more source

Hearing and Balance Problems in a Chiari-1 Malformation Associated with Communicating Hydrocephalus - A Case Report [PDF]

Chiari malformation is characterized by an anatomical alteration at the base of the skull, cerebellar herniation, or brainstem herniation via the magnum foramen and up to the cervical spinal canal. It is categorized into five subtypes from type 0 to type
Pavan K, Sabarish A
core   +1 more source