European academy of andrology guidelines on Klinefelter Syndrome: Endorsing Organization: European Society of Endocrinology

dc.contributor.authorMichael Zitzmann
dc.contributor.authorLise Aksglaede
dc.contributor.authorGiovanni Corona
dc.contributor.authorAndrea M. Isidori
dc.contributor.authorAnders Juul
dc.contributor.authorGuy T'Sjoen
dc.contributor.authorSabine Kliesch
dc.contributor.authorKathleen D'Hauwers
dc.contributor.authorJorma Toppari
dc.contributor.authorJolanta Słowikowska-Hilczer
dc.contributor.authorFrank Tüttelmann
dc.contributor.authorAlberto Ferlin
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=lastentautioppi|en=Paediatrics and Adolescent Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organizationfi=väestötutkimuskeskus|en=Centre for Population Health Research (POP Centre)|
dc.contributor.organization-code1.2.246.10.2458963.20.42471027641
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id50622450
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/50622450
dc.date.accessioned2022-10-28T14:18:39Z
dc.date.available2022-10-28T14:18:39Z
dc.description.abstractBackground Knowledge about Klinefelter syndrome (KS) has increased substantially since its first description almost 80 years ago. A variety of treatment options concerning the spectrum of symptoms associated with KS exists, also regarding aspects beyond testicular dysfunction. Nevertheless, the diagnostic rate is still low in relation to prevalence and no international guidelines are available for KS. <div>Objective To create the first European Academy of Andrology (EAA) guidelines on KS. </div><div>Methods An expert group of academicians appointed by the EAA generated a consensus guideline according to the GRADE (Grading of Recommendations, Assessment, Development and Evaluation) system. </div><div>Results Clinical features are highly variable among patients with KS, although common characteristics are severely attenuated spermatogenesis and Leydig cell impairment, resulting in azoospermia and hypergonadotropic hypogonadism. In addition, various manifestations of neurocognitive and psychosocial phenotypes have been described as well as an increased prevalence of adverse cardiovascular, metabolic and bone-related conditions which might explain the increased morbidity/mortality in KS. Moreover, compared to the general male population, a higher prevalence of dental, coagulation and autoimmune disorders is likely to exist in patients with KS. Both genetic and epigenetic effects due to the supernumerary X chromosome as well as testosterone deficiency contribute to this pathological pattern. The majority of patients with KS is diagnosed during adulthood, but symptoms can already become obvious during infancy, childhood or adolescence. The paediatric and juvenile patients with KS require specific attention regarding their development and fertility. </div><div>Conclusion These guidelines provide recommendations and suggestions to care for patients with KS in various developmental stages ranging from childhood and adolescence to adulthood. This advice is based on recent research data and respective evaluations as well as validations performed by a group of experts.</div>
dc.identifier.eissn2047-2927
dc.identifier.jour-issn2047-2919
dc.identifier.olddbid187522
dc.identifier.oldhandle10024/170616
dc.identifier.urihttps://www.utupub.fi/handle/11111/39584
dc.identifier.urnURN:NBN:fi-fe2021042826033
dc.language.isoen
dc.okm.affiliatedauthorToppari, Jorma
dc.okm.affiliatedauthorDataimport, Lastentautioppi
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA2 Scientific Article
dc.publisherWILEY
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1111/andr.12909
dc.relation.ispartofjournalAndrology
dc.relation.issue1
dc.relation.volume9
dc.source.identifierhttps://www.utupub.fi/handle/10024/170616
dc.titleEuropean academy of andrology guidelines on Klinefelter Syndrome: Endorsing Organization: European Society of Endocrinology
dc.year.issued2020

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