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European academy of andrology guidelines on Klinefelter syndrome : endorsing organization : European Society of Endocrinology
- Source :
- ANDROLOGY, Andrology, 9, 145-167, Andrology, 9, 1, pp. 145-167, Zitzmann, M, Aksglaede, L, Corona, G, Isidori, A M, Juul, A, T'Sjoen, G, Kliesch, S, D'Hauwers, K, Toppari, J, Słowikowska-Hilczer, J, Tüttelmann, F & Ferlin, A 2021, ' European academy of andrology guidelines on Klinefelter Syndrome Endorsing Organization : European Society of Endocrinology ', Andrology, vol. 9, no. 1, pp. 145-167 . https://doi.org/10.1111/andr.12909
- Publication Year :
- 2021
-
Abstract
- Contains fulltext : 245049.pdf (Publisher’s version ) (Open Access) BACKGROUND: 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. OBJECTIVE: To create the first European Academy of Andrology (EAA) guidelines on KS. 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. 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. 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.
- Subjects :
- Klinefelter syndrome
guidelines
hypergonadotropic hypogonadism
azoospermia
Urology
Endocrinology, Diabetes and Metabolism
media_common.quotation_subject
ANTI-MULLERIAN HORMONE
Fertility
MALE BREAST-CANCER
Andrology
03 medical and health sciences
Klinefelter Syndrome
0302 clinical medicine
Endocrinology
Hypergonadotropic hypogonadism
medicine
Medicine and Health Sciences
SEX-CHROMOSOME ABNORMALITIES
Humans
Pathological
media_common
METABOLIC SYNDROME
Azoospermia
030219 obstetrics & reproductive medicine
business.industry
TESTICULAR SPERM EXTRACTION
ANDROGEN RECEPTOR
medicine.disease
Reconstructive and regenerative medicine Radboud Institute for Health Sciences [Radboudumc 10]
Reproductive Medicine
X-CHROMOSOME
XXY KLINEFELTER
Metabolic syndrome
BONE-MINERAL DENSITY
business
TESTOSTERONE REPLACEMENT THERAPY
Psychosocial
Neurocognitive
Subjects
Details
- Language :
- English
- ISSN :
- 20472919 and 20472927
- Database :
- OpenAIRE
- Journal :
- ANDROLOGY, Andrology, 9, 145-167, Andrology, 9, 1, pp. 145-167, Zitzmann, M, Aksglaede, L, Corona, G, Isidori, A M, Juul, A, T'Sjoen, G, Kliesch, S, D'Hauwers, K, Toppari, J, Słowikowska-Hilczer, J, Tüttelmann, F & Ferlin, A 2021, ' European academy of andrology guidelines on Klinefelter Syndrome Endorsing Organization : European Society of Endocrinology ', Andrology, vol. 9, no. 1, pp. 145-167 . https://doi.org/10.1111/andr.12909
- Accession number :
- edsair.doi.dedup.....53e3f81c5393564fc22e33b0c07f9b29
- Full Text :
- https://doi.org/10.1111/andr.12909