La sindrome di Turner

di riferimento • Bergamaschi R, Bergonzoni C, Mazzanti L, et al. Hearing loss in Turner syndrome: results of a multicentric study. J Endocrinol Invest 2008;31:779-83.doi: 10.1007/BF03349257. • Bondy C, Bakalov VK, Cheng C, Olivieri L, Rosing DR, Arain AE. Bicuspid aortic valve and aortic coartaction are linked to deletion of the X chromosome short arm in Turner syndrome. J Med Genet 2013;50:662-5. doi: 10.1136/jmedgenet-2013-101720. • Calcaterra V, Brambilla P, Maffè GC, et al. Metabolic syndrome in Turner syndrome and relation between body composition and clinical, genetic, and ultrasonographic characteristics. Metab Syndr Relat Disord 2014;12:159-64. doi: 10.1089/met.2013.0075. • Davenport ML. Approach to the patient with Turner syndrome. J Clin Endocrinol Metab 2010;95:1487-95. doi: 10.1210/jc.2009-0926. • Donaldson MD, Gault EJ, Tan KW, Dunger DB. Optimising management in Turner syndrome: from infancy to adult transfer. Arch Dis Child 2006;91:513-20. doi: 10.1136/adc.2003.035907. • Gonzalez L, Feldman Witchel S. The patient with Turner syndrome: puberty and medical management concerns. Fertility and Sterility 2012;98(4). doi: 10.1016/j.fertnstert.2012.07.1104. • Gravholt CH, Andersen NH, Conway GS, et al. International Turner Syndrome Consensus Group. Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting. Eur J Endocrinol 2017;177(3):G1-G70. doi: 10.1530/EJE-17-0430. • Levitsky LL, Luria AH, Hayes FJ, Lin AE. Turner syndrome: update on biology and management across the life span. Curr Opin Endocrinol Diabetes Obes 2015;22:65-72. doi: 10.1097/MED. 0000000000000128. • Salomone R, Chiarelli F. Gestione della sindrome di Turner in età pediatrica e durante la vita adulta. Medico e Bambino 2008;27: 157-65. • Sybert VP, McCauley E. Turner’s syndrome. N Engl J Med 2004; 351:1227-38. doi: 10.1056/NEJMra030360.