Abstract
Motility disorders often complicate the medical history of primary diseases. High prevalences of gastroesophageal reflux disease (GERD) and swallowing disorders are described in patients affected by cerebral palsy, familial dysautonomia, and Williams syndrome; Down syndrome has been associated with a high incidence of GERD and Hirschsprung disease, and many gastrointestinal complaints have been described in patients affected by mitochondrial disorders. Gastrointestinal motility problems represent an important cause of morbidity and sometimes mortality in patients affected by developmental disorders. Nevertheless, they are often neglected because priority is mainly given to other clinical aspects of these pathologies. However, early diagnosis and optimal care is required to improve the quality of life and minimize morbidity and mortality of these patients.
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Staiano, A., Martinelli, M. (2013). Motility Problems in Developmental Disorders: Cerebral Palsy, Down Syndrome, William Syndrome, Familial Dysautonomia, and Mitochondrial Disorders. In: Faure, C., Di Lorenzo, C., Thapar, N. (eds) Pediatric Neurogastroenterology. Clinical Gastroenterology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-60761-709-9_24
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