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. 2016 Jun 2;12:873–881. doi: 10.2147/TCRM.S70068

Table 2.

Growth hormone for Prader–Willi syndrome: challenges for future research

Pediatric age
Optimal dosage of GH therapy
Effects of GH treatment in children born SGA (compared to AGA)
Clinical impact of GHD on GH therapeutical response
Transition phase
Evaluation of GH secretory pattern with respect to the clinical response of subsequent GH therapy
Clinical effects of GH therapy early after completion of linear growth and influence of GH secretory status
Adult age (≥25 years)
Evaluation of GH secretory pattern with respect to the clinical response of subsequent GH therapy
Influence of GH therapy in non-GH-deficient patients
Cardiovascular and respiratory effects of GH treatment
All ages
Long-term surveillance of benefits and risks of GH replacement, including risk of neoplasia
Genotype–phenotype correlation and GH therapy
Role of GH therapy on bone health
Role of concomitant therapies on GH therapeutic effects (sex steroids, diet, physical therapy, etc)

Abbreviations: GH, growth hormone; SGA, small for gestational age; AGA, appropriate for gestational age; GHD, GH deficiency.