
Recombinant human growth hormone, synthesized in E.coli or mammalian cells cultures, is since 1985, a useful therapeutic resource to increase growth velocity and final height. In this paper are discussed the four phases (aims, security and efficacy, utility and efficiency) indispensables to define the start of treatment, as well as the absolute, relative and metabolic indications and the transitory and permanent conditions that contraindicate its use. It is commented the way to optimize the results (simple but indispensables indications for the physician, the patients and their family). Finally it is analyzed the results of treatment in patients with growth hormone deficiency, Turner syndrome, chronic renal failure, Prader-Willi syndrome, Noonan syndrome, SHOX deficiency, intrauterine growth retardation and idiopathic short stature.
Fetal Growth Retardation, Human Growth Hormone, Noonan Syndrome, Contraindications, Drug, Turner Syndrome, Dwarfism, Drug Administration Schedule, Recombinant Proteins, Treatment Outcome, Humans, Renal Insufficiency, Chronic, Prader-Willi Syndrome, Growth Disorders
Fetal Growth Retardation, Human Growth Hormone, Noonan Syndrome, Contraindications, Drug, Turner Syndrome, Dwarfism, Drug Administration Schedule, Recombinant Proteins, Treatment Outcome, Humans, Renal Insufficiency, Chronic, Prader-Willi Syndrome, Growth Disorders
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