Rongen-Westerlaken C, Wit J M
Afd. Kindergeneeskunde, Academisch Ziekenhuis Nijmegen, St. Radboud Ziekenhuis.
Tijdschr Kindergeneeskd. 1992 Oct;60(5):155-63.
Short stature is a feature in almost all cases with Turner syndrome. The etiology is unknown, but GH secretion appears to be normal. The treatment with anabolic steroids does not seem to increase final height. Oestrogens are needed for secondary sex characteristics, but should be given in a low dosage and at approximately 12-13 years of age, in order not to compromise final height. Growth hormone increases growth velocity and leads to an average gain of 5 cm in terms of final height. The addition of oxandrolone leads to an even higher growth rate, but final height is probably similar to that reached by growth hormone alone. The dosage, injection frequency, age and bone age at the start of therapy have influence on the efficacy. GH in the dosages given appears safe.
身材矮小几乎是所有特纳综合征病例的一个特征。病因不明,但生长激素分泌似乎正常。使用合成代谢类固醇进行治疗似乎不会增加最终身高。继发性征需要雌激素,但应低剂量给药,且大约在12 - 13岁时给药,以免影响最终身高。生长激素可提高生长速度,最终身高平均增加5厘米。加用氧雄龙可使生长速度更高,但最终身高可能与仅使用生长激素时相似。治疗开始时的剂量、注射频率、年龄和骨龄会影响疗效。所给剂量的生长激素似乎是安全的。