首页> 外文期刊>Pediatric Research >13 EVALUTION OF THE EFFICACY OF GROWTH HORMONE TREATMENT WITH RECOMBINANT HUMAN GROWTH HORMONE |[lpar]|rhGH|[rpar]| IN |[ldquo]|SHORT NORMAL|[rdquo]| CHILDREN WITHOUT GH DEFICIENCY
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13 EVALUTION OF THE EFFICACY OF GROWTH HORMONE TREATMENT WITH RECOMBINANT HUMAN GROWTH HORMONE |[lpar]|rhGH|[rpar]| IN |[ldquo]|SHORT NORMAL|[rdquo]| CHILDREN WITHOUT GH DEFICIENCY

机译:| 13重组人生长激素| lpar | rhGH | rpar |治疗生长激素的疗效评估在| [ldquo] |短正常| [rdquo] |缺乏GH的儿童

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Some children with GH deficiency on tests fro grewth hormone secretion and with normal laboratory evaluation for short stature, present abnormal growth velocity (GV) or predict adult height (PAH) balcw the target height (TH); probably they will not attain a final height in accordance with their genetical potential. We studied 14 of those children: 8 boys and 6 girls, ages between 8 and 12.4 years (14=10.0 y). Eight children were classified as familial short stature and 4 as “idiopathic” short stature: 2 other had abnormal GV. rhGH, 1 U/kg/week, SC, in daily dosis was given. Six children with pubertal signs (Tanner stages II and III) ware treated concomitantly with long acting LH-RH analog (Decapeptyl 3 mg, IM, monthly). The results of the treatment at 6 (14 patients) and at 12 months (5 patients) were:No side effects were observed and TSH, T4, T3, glyomia and urine analysis were normal. In agreement with literature these results suggest that to some “short normal” children the use of rhGH could increase the final height.
机译:一些生长激素缺乏症的儿童生长激素分泌检查,身材矮小,实验室检查正常,表现出异常的生长速度(GV)或预测成年身高(PAH)不能达到目标身高(TH)。他们可能无法根据其遗传潜能达到最终高度。我们研究了其中的14个孩子:8个男孩和6个女孩,年龄在8到12.4岁之间(14 = 10.0岁)。有8名儿童被归为家族性矮小,有4名为“特发性”矮小:另外2名GV异常。每日剂量为rhGH,1 U / kg /周,SC。六个有青春期体征的孩子(坦纳期II和III期)应与长效LH-RH类似物(十肽3 mg,IM,每月)一起治疗。 6例(14例患者)和12个月(5例患者)的治疗结果是:未观察到副作用,TSH,T4,T3,乙二醛和尿液分析均正常。与文献一致的是,这些结果表明,对于某些“矮正常”儿童,使用rhGH可能会增加最终身高。

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