FOXP1 Syndrome and Severe Obstructive Sleep Apnea

J Clin Sleep Med. 2018 Aug 15;14(8):1432-1434. doi: 10.5664/jcsm.7292.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child Behavior Disorders / complications*
  • Child Behavior Disorders / genetics
  • Child, Preschool
  • Continuous Positive Airway Pressure
  • Developmental Disabilities / complications*
  • Developmental Disabilities / genetics
  • Diagnosis, Differential
  • Forkhead Transcription Factors / genetics*
  • Humans
  • Male
  • Megalencephaly / complications*
  • Megalencephaly / genetics
  • Mutation / genetics
  • Otitis Media / complications*
  • Otitis Media / genetics
  • Polysomnography
  • Repressor Proteins / genetics*
  • Sleep Apnea, Obstructive / complications*
  • Sleep Apnea, Obstructive / diagnosis
  • Sleep Apnea, Obstructive / genetics
  • Sleep Apnea, Obstructive / therapy
  • Syndrome

Substances

  • FOXP1 protein, human
  • Forkhead Transcription Factors
  • Repressor Proteins