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Adapting Human Videofluoroscopic Swallow Study Methods to Detect and Characterize Dysphagia in Murine Disease Models
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Dysphagia in infantile cortical hyperostosis (Caffey's disease): a case study

J J Sheppard1, H Pressman

  • 1Teachers College, Columbia University, NJ.

Developmental Medicine and Child Neurology
|February 1, 1988
PubMed

Insights

Infantile cortical hyperostosis (Caffey's disease) can cause infant dysphagia. Continued therapeutic oral feeding alongside nutritional support aids oral feeding skills and infant-parent bonding.

Area of Science:

  • Pediatrics
  • Gastroenterology
  • Genetics

Background:

  • Infantile cortical hyperostosis, also known as Caffey's disease, is a rare disorder characterized by bone overgrowth.
  • Dysphagia, or difficulty swallowing, is a common symptom in infants with Caffey's disease, often leading to feeding refusal and failure to thrive.

Observation:

  • A four-month-old infant diagnosed with Caffey's disease presented with significant dysphagia.
  • Nutritional support was provided via nasal or gastrostomy intubation.
  • Therapeutic oral feeding was concurrently administered.

Findings:

  • The combined approach of nutritional support and therapeutic oral feeding facilitated the development of oral feeding skills in the infant.
  • This management strategy also promoted positive infant-parent bonding and the infant's experience of oral satisfaction.

Implications:

  • Early and continued intervention focusing on oral feeding can mitigate the effects of dysphagia in infants with Caffey's disease.
  • This approach highlights the importance of addressing both nutritional needs and developmental milestones in managing complex pediatric conditions.

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