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

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....

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Bibliographic Details
Main Authors: Alberto Spalice (Author), Luigi Tarani (Author), Francesca Del Balzo (Author), Francesco Costantino (Author), Enrico Properzi (Author), Natascia Liberato (Author)
Format: Book
Published: MDPI AG, 2010-09-01T00:00:00Z.
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Summary: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.
Item Description:2036-749X
2036-7503
10.4081/pr.2010.e8