Neonatal stridor presents at home – vocal fold paralysis as rare presenting feature of charge syndrome

HIGHLIGHTS

• who: Suhagi M. Kadakia from the University Medical Center, Chicago, IL, USA have published the paper: Neonatal stridor presents at homeu00a0u2013 vocal fold paralysis as rare presenting feature of CHARGE syndrome, in the Journal: (JOURNAL)

SUMMARY

CHARGE syndrome is an autosomal dominant disorder that most often results from de novo mutations in the CHD7 (chromodomain helicase DNA binding protein 7) gene. Other upper airway anomalies associated with CHARGE syndrome include tracheomalacia, tracheoesophageal fistula, laryngomalacia, subglottic stenosis, and laryngeal clefts. [2, 3] Association with vocal fold paralysis (VFP) has been reported in the literature . . .

 



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