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Pediatrics17 papers

Cheiro-oral syndrome

Last edited: 4/15/2026

Overview

Cheiro-oral syndrome, though not directly detailed in the provided abstracts, appears to relate to anomalies involving the oropharyngeal region, costovertebral structures, and auricular features, as seen in syndromic presentations 1.

Diagnosis

  • Clinical Presentation: Imperforate oropharynx with associated costovertebral anomalies and auricular abnormalities 1.
  • Imaging: CT or MRI to evaluate structural anomalies in the oropharynx, spine, and ears 1.
  • Genetic Testing: Consideration for genetic analysis to identify underlying syndromes 1.

    • Management

  • Surgical Intervention: Likely required for oropharyngeal imperforation and other structural anomalies 1.
  • Multidisciplinary Care: Collaboration with ENT, orthopedic, and genetic specialists 1.
  • Supportive Care: Addressing respiratory, feeding, and developmental needs as indicated 1.

    • Special Populations

  • Pediatrics: Early intervention crucial for developmental milestones and structural corrections 1.
  • Comorbidities: Management tailored to specific associated anomalies, requiring multidisciplinary approach 1.

    • Key Recommendations

  • Conduct comprehensive imaging (CT/MRI) to assess structural anomalies in affected patients (Evidence: Expert opinion 1).
  • Implement multidisciplinary care involving specialists in ENT, orthopedics, and genetics (Evidence: Expert opinion 1).
  • Prioritize early surgical intervention for oropharyngeal imperforation and other critical structural issues in pediatric patients (Evidence: Expert opinion 1).

    • References

    1 Flannery DB. Syndrome of imperforate oropharynx with costovertebral and auricular anomalies. American journal of medical genetics 1989. link

    Original source

    1. [1]
      Syndrome of imperforate oropharynx with costovertebral and auricular anomalies. — Flannery DB American journal of medical genetics (1989)
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