Neuromuscular disorders presenting as congenital bilateral vocal cord paralysis

J F Lapeña1, R G Berkowitz

  • 1Department of Otolaryngology, Royal Children's Hospital, Melbourne, Australia.

Insights

Congenital bilateral vocal cord paralysis (BVCP) in infants may indicate an underlying, yet undiagnosed, neuromuscular disorder. Early recognition of BVCP is crucial for timely diagnosis and management of these serious conditions.

Area of Science:

  • Pediatric Neurology
  • Otolaryngology
  • Genetics

Background:

  • Congenital bilateral vocal cord paralysis (BVCP) is a rare condition affecting infants.
  • It can be an early or isolated sign of underlying neuromuscular disorders.

Observation:

  • A study followed infants under 12 months with BVCP diagnosed before other neuromuscular symptoms.
  • Three cases presented with airway obstruction at birth, diagnosed via laryngoscopy without structural laryngeal abnormalities.

Findings:

  • Subsequent diagnoses included facioscapulohumeral myopathy, spinal muscular atrophy, and congenital myasthenia gravis.
  • Neuromuscular symptoms appeared 4 months to 7 years after BVCP diagnosis.
  • Prognosis for BVCP symptoms correlated with the primary neuromuscular disorder.

Implications:

  • Congenital BVCP warrants consideration as a potential early indicator of unrecognized neuromuscular conditions.
  • Investigate for neuromuscular disorders in infants with BVCP, especially with progressive symptoms or associated dysfunction.
  • This highlights the importance of a multidisciplinary approach in diagnosing and managing pediatric airway and neurological conditions.

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