Sommario
La sindrome di Klinefelter (KS) è caratterizzata da disgenesia testicolare ed associata ad uno o più cromosomi X sovranumerari. Oltre al quadro di ipogonadismo ipergonadotropo, ad oggi, nei pazienti KS è stata dimostrata una maggiore predisposizione verso processi autoimmuni caratteristici dell’artrite reumatoide, polimiosite e dermatomiosite, lupus eritematoso sistemico, sclerosi sistemica, alterazioni miste del connettivo (MCTD), diabete di tipo 1 e tiroidite di Hashimoto.
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Gli autori Antonio F. Radicioni e Francesca Panimolle dichiarano di non avere conflitti di interesse.
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Radicioni, A.F., Panimolle, F. Sindrome di Klinefelter e autoimmunità. L'Endocrinologo 18, 159–164 (2017). https://doi.org/10.1007/s40619-017-0342-y
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DOI: https://doi.org/10.1007/s40619-017-0342-y