Abstract
Cyclic vomiting syndrome (CVS) diagnosis has been facilitated by the recently defined consensus diagnostic criteria by NASPGHAN (2008), Rome III (2006), Rome IV, and International Headache Society (2013) criteria. This chapter focuses on the most recent data on comorbidities and clinical subphenotypes, pathophysiologic pathways, and new therapeutic avenues. Despite improved characterization, recognition, and understanding of CVS in the past two decades, without a delineated pathophysiologic cascade, it remains classified as a functional gastrointestinal disorder. Although originally perceived to be a pediatric disorder, the past decade has been witness to a dramatic rise in diagnosed adults. In both children and adults, the hallmark symptoms described by Samuel Gee in 1882 remain applicable today and include stereotypical, severe episodes of vomiting punctuating symptom-free periods, or baseline health [1]. Recent work has begun to expand the list of comorbidities and clinical subphenotypes and identify pathophysiologic pathways and new therapeutic avenues.
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Acknowledgment
We would like to acknowledge Dr. Bhanu Sunku who contributed substantively to the chapter in the previous edition.
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Li, B.U.K., Kovacic, K. (2017). Cyclic Vomiting Syndrome: Comorbidities and Treatment. In: Faure, C., Thapar, N., Di Lorenzo, C. (eds) Pediatric Neurogastroenterology. Springer, Cham. https://doi.org/10.1007/978-3-319-43268-7_39
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DOI: https://doi.org/10.1007/978-3-319-43268-7_39
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