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Growth hormone treatment in Turner syndrome accelerates growth and skeletal maturation

  • Endocrinology
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Abstract

Sixteen girls with Turner syndrome (TS) were treated for 4 years with biosynthetic growth hormone (GH). The dosage was 4IU/m2 body surface s.c. per day over the first 3 years. In the 4th year the dosage was increased to 61 U/m2 per day in the 6 girls with a poor height increment and in 1 girl oxandrolone was added. Ethinyl oestradiol was added after the age of 13. Mean (SD) growth velocities were 3.4 (0.9), 7.2 (1.7), 5.3 (1.3), 4.3 (2.0) and 3.6 (1.5) cm/year before and in the 1st, 2nd, 3rd and 4th year of treatment. Skeletal maturation advanced faster than usual in Turner patients especially in the youger children. Although the mean height prediction increased by 5.6 cm and 11 of the 16 girls have now exceeded their predicted height, the height of the 4 girls who stopped GH treatment exceeded the predicted adult height by only 0 to 3.4 cm.

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Abbreviations

GH:

growth hormone

GP:

Greulich and Pyle

TS:

Turner syndrome

TW-RUS:

Bone age according to the method of Tanner and Whitehouse (Radius, ulna and short bones

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Rongen-Westerlaken, C., Wit, J.M., De Muinck Keizer-Schrama, S.M.P.F. et al. Growth hormone treatment in Turner syndrome accelerates growth and skeletal maturation. Eur J Pediatr 151, 477–481 (1992). https://doi.org/10.1007/BF01957747

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  • DOI: https://doi.org/10.1007/BF01957747

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