Late-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report. [electronic resource]
Producer: 20130502Description: 951-5 p. digitalISSN:- 1522-1709
- Adolescent
- Child
- Child, Preschool
- Continuous Positive Airway Pressure
- DNA Mutational Analysis
- DNA Repeat Expansion -- genetics
- Follow-Up Studies
- Homeodomain Proteins -- genetics
- Humans
- Hypoventilation -- congenital
- Infant
- Infant, Newborn
- Male
- Middle Aged
- Patient Compliance
- Phenotype
- Polysomnography
- Recurrence
- Respiratory Distress Syndrome, Newborn -- diagnosis
- Sleep Apnea, Central -- diagnosis
- Tracheotomy
- Transcription Factors -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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