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Journal of Pediatric Neurology 2014; 12(01): 049-053
DOI: 10.3233/JPN-140638
DOI: 10.3233/JPN-140638
Case Report
Intractable hiccups as a presenting feature of clinically isolated syndrome
Verantwortlicher Herausgeber dieser Rubrik:
Weitere Informationen
Publikationsverlauf
12. Dezember 2012
21. September 2013
Publikationsdatum:
30. Juli 2015 (online)
Abstract
We report a 15-year-old girl with intractable hiccups unresponsive to high doses of proton pump inhibitors. Further investigations revealed an acute demyelinating neurological disorder on magnetic resonance imaging of the brain with a lesion in the brain stem responsible for the hiccups. Hiccups are a common and usually transient condition. It is rare for it to become intractable. Persistent hiccups may reflect a serious underlying disease, as in our case due to a demyelinating disorder. We would like to highlight the underlying causes of an acute demyelinating neurological disorder and the characteristics to help with the differential diagnosis.