Abstract |
Oropharyngeal dysphagia can cause chronic aspiration leading to significant respiratory symptoms. When dysphagia is diagnosed, an underlying cause is sought. We present a case series of 15 children diagnosed aged 6 months to 5 years (mean 2y 5mo; 11 males, four females) over a 6-year period, who were found to have an isolated bulbar palsy on genioglossus electromyography, with no accompanying neurological or neurodevelopmental disorder. Eight children had dysphagia but a normal EMG. In those with isolated bulbar palsy, management included thickened fluids (n=13), cooled boiled water (n=1), and nasogastric tube feeding (n=1). Follow-up over 1 to 8 years (mean 5y) showed complete resolution in six children, improvement in four children, and no improvement in five children (including two requiring fluids via a gastrostomy). Eight children no longer had any respiratory symptoms. Isolated bulbar palsy is under-recognized and has not been reported previously as a cause of significant dysphagia in children.
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Authors | Stacey Zimmels, Ian M Balfour-Lynn, Loucas Christodoulou, Mantha Pantazi, Efterpi Pavlidou, Matthew Pitt, Maria Kinali, Naila Ismayilova |
Journal | Developmental medicine and child neurology
(Dev Med Child Neurol)
Vol. 64
Issue 4
Pg. 518-522
(04 2022)
ISSN: 1469-8749 [Electronic] England |
PMID | 34601721
(Publication Type: Case Reports, Journal Article)
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Copyright | © 2021 Mac Keith Press. |
Topics |
- Bulbar Palsy, Progressive
(complications, therapy)
- Child
- Deglutition Disorders
(diagnosis, etiology, therapy)
- Electromyography
(adverse effects)
- Female
- Gastrostomy
- Humans
- Male
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