Adenotosillar hypertrophy |
Obesity |
Subtle craniofacial abnormalities or profound craniofacial anomalies |
Mild mandibular retrognathia |
Marked midfacial hypoplasia (e.g. Apert syndrome, Crouzon syndrome) |
Marked mandibular hypoplasia (e.g. Pierre Robin sequence, Treacher Collins syndrome, Stickler syndrome) |
Mucopolysacharidoses |
Abnormal neuromotor tone and/or control of breathing |
Cerebral palsy |
Duchenne muscular dystrophy |
Combinations of the above disorders or conditions |
Down's syndrome |
Achondroplasia |
Prader-Willi syndrome |