FOXP1 Syndrome and Severe Obstructive Sleep Apnea

J Clin Sleep Med. 2018 Aug 15;14(8):1432-1434. doi: 10.5664/jcsm.7292.

Authors

Ilia Kritikou¹, Olufunke Afolabi-Brown^{1

2}

Affiliations

¹ Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
² Department of Pulmonary and Sleep Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

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