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. 2019 Nov;15(4):207–244. doi: 10.2174/1573396315666190716120925

Table 1. Table of contents.

INTRODUCTION 207
Key Points 208
Background 209
MATERIALS AND METHOD 211
RESULTS AND DISCUSSION 211
Epidemiology 211
Causes and Risk Factors 211
Associated Disorders Ordered by Importance 212
Complications Related to Prader-Willi Syndrome 213
Population at Risk or Screening Modalities 213
Preventive Measures 213
Clinical Presentation and Testing 213
Clinical Consensus Diagnostic Criteria 215
Laboratory Evaluation 215
Specific Genetic Laboratory Tests 217
Specific Clinic Testing 219
Other Obesity-related Disorders 221
Consultation for Diagnosis 224
Treatment and Medications 224
Vitamins and Other Supplements 232
Non-drug Treatments 233
CONCLUSION 236
Patient Satisfaction/Lifestyle Priorities 236
Consultation 236
Monitoring 237
Prognosis 237
Complications 238
Secondary Prevention/Patient Education 238
Practice Performance Measures/Summary of Evidence 239
Guidelines 239
Diagnostic Codes (ICD9-759.81 and ICD10-Q87.1) for Prader-Willi Syndrome 240
Clinical and Parent Questions 240
CONFLICT OF INTEREST 241
ACKNOWLEDGEMENTS 241
DISCLOSURE 241
REFERENCES 241