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. © L. Tarani et al., 2010.
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Tarani, L., Del Balzo, F., Costantino, F., Properzi, E., D’Eufemia, P., Liberati, N., & Spalice, A. (2010). Chiari type I malformation, syncope, headache, hypoglycemia and hepatic steatosis in an 8-year old girl: A causal association? Pediatric Reports, 2(1), 26–28. https://doi.org/10.4081/pr.2010.e8
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