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生长激素缺乏患者在接受人生长激素治疗前的人体测量。

Anthropometric measurements in patients with growth hormone deficiency before treatment with human growth hormone.

作者信息

Zachmann M, Fernandez F, Tassinari D, Thakker R, Prader A

出版信息

Eur J Pediatr. 1980 May;133(3):277-82. doi: 10.1007/BF00496089.

Abstract

In 74 children (52 males, 22 females) with growth hormone (GH) deficiency (30 cases with isolated GH-deficiency, two of them familial; 4 familial and one isolated case with tendency for formation of antibodies against hGH; 29 with other pituitary hormone defects; 10 craniopharyngiomas), various anthropometric measurements were analyzed before treatment with hGH. In all groups, standing height, sitting height, and subischial leg height were equally retarded, and bihumeral width was more retarded than biiliac width; the head was relatively large; fat tissue was increased with subscapular skinfolds being greater than triceps skinfolds, indicating relative obestiy of the trunk; muscle and/or bone mass was reduced. In isolated GH-deficiency, head shape was slightly scaphoid; in combined defects, it was round, and in craniopharyngioma cases, it was brachycephalic. It is concluded that antrhopometric measurements may help in differentiating the type of GH-deficiency.

摘要

对74例生长激素(GH)缺乏症患儿(52例男性,22例女性)(30例单纯性GH缺乏症,其中2例为家族性;4例家族性及1例单纯性病例有产生抗hGH抗体的倾向;29例有其他垂体激素缺陷;10例颅咽管瘤)在使用hGH治疗前进行了各种人体测量分析。在所有组中,身高、坐高和坐骨下腿高同样发育迟缓,双肱骨宽度比双髂嵴宽度发育迟缓更明显;头部相对较大;脂肪组织增加,肩胛下皮褶大于肱三头肌皮褶,表明躯干相对肥胖;肌肉和/或骨量减少。在单纯性GH缺乏症中,头部形状略呈舟状;在合并缺陷中,头部呈圆形,在颅咽管瘤病例中,头部呈短头型。结论是人体测量可能有助于区分GH缺乏症的类型。

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