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Chiari type I malformation, syncope, headache, hypoglycemia and hepatic steatosis in an 8-year old girl: a causal association?

By Luigi Tarani, Francesca Del Balzo, Francesco Costantino, Enrico Properzi, Patrizia D’Eufemia, Natascia Liberati and Alberto Spalice

Abstract

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

Topics: Case Report
Publisher: PAGEPress Publications
OAI identifier: oai:pubmedcentral.nih.gov:3094011
Provided by: PubMed Central

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Citations

  1. Asymptomatic Chiari Type I Case Report
  2. Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients.
  3. (2006). Posterior fossa volume in children with Chiari malformation Type I.