Multidisciplinary care in the intensive care unit for a patient with Prader-Willi syndrome: a dental approach

Insights

Prader-Willi syndrome (PWS) can cause severe oral health issues, including ulcerations linked to herpes. Early diagnosis and multidisciplinary care can significantly improve outcomes for PWS patients.

Area of Science:

  • Genetics
  • Neuroscience
  • Pediatrics

Background:

  • Prader-Willi syndrome (PWS) is a complex genetic disorder impacting development.
  • PWS is associated with obesity, hypotonia, endocrine, and cognitive issues.
  • Oral integrity can be compromised in individuals with PWS.

Purpose of the Study:

  • To report a case of a 15-year-old male with PWS presenting with significant oral manifestations.
  • To investigate the etiology of oral ulcerations in this PWS patient.
  • To emphasize the importance of early diagnosis and intervention in managing PWS.

Main Methods:

  • Clinical oral examination of a 15-year-old PWS patient.
  • Assessment of oral hygiene, occlusion, and salivary characteristics.
  • Excision biopsy of oral ulcerations for histopathological analysis.

Main Results:

  • The patient exhibited bacterial plaque, gingivitis, poor occlusion, and viscous salivation.
  • Multiple ulcerations were found on the lips, jugal mucosa, gums, and tongue.
  • Biopsy revealed herpes-typical ulcerations, potentially linked to herpes encephalitis.

Conclusions:

  • Oral ulcerations in PWS patients may be associated with herpes infections.
  • Prompt diagnosis and early therapeutic interventions can mitigate PWS complications.
  • Integrated, multidisciplinary care is crucial for effective PWS patient management.

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