Introduction: Klinefelter syndrome brings together all the clinical and hormonal manifestations linked to the presence of a supernumerary X chromosome, giving a classical karyotype of 47, XXY. It is a genetic disease, the leading cause of aneuploidy in humans, making it one of the most common chromosomal diseases. The association with diabetes is rare resulting from multiple pathophysiological mechanisms. Observation: We report the case of a 47-year-old patient with a history of familial diabetes hospitalized for initial decompensation of his diabetes in the ketoacidotic mode who also presented a clinical picture of hypogonadism with a gynoid morphotype, a micropenis, a bilateral gynecomastia, female pubic hair associated with testicular atrophy in a context of couple infertility. The picture suggested Klinefelter syndrome associated with type 2 diabetes confirmed by hormonal (hypergonadotropic hypogondism) and genetic (47XXY karyotype) explorations. Conclusion: Klinefelter syndrome is a common cause of hypogonadism and male infertility. It is often diagnosed late. The association with diabetes is possible under the influence of multiple physiopathological mechanisms. We must think about this syndrome in the face of any hypergonadotropic hypogonadism and have an easy karyotype in this context.
References
[1]
Klinefelter, H.F.R.E. and Albright, F. (1942) Syndrome caractérisé par une gynécomastie, une aspermatogenèse sans A-Leydigisme et une excrétion accrue de l’hormone follicu-lo-stimulante. The Journal of Clinical Endocrinology & Metabolism, 2, 615-627.
[2]
Bonomi, M., Rochira, V., Pasquali, D., Balercia, G., Jannini, E.A. and Ferlin, A. (2016) Klinefelter Syndrome (KS): Genetics, Clinical Phenotype and Hypogonadism. JournalofEndocrinologicalInvestigation, 40, 123-134. https://doi.org/10.1007/s40618-016-0541-6
[3]
Mariko, M.L., Bah, M., Maiga, M.M., Sow, D.S., Mariko, M., Togo, A., et al. (2016) Gynécomastie bilatérale révélant un syndrome de Klinefelter chez un militaire à l’hôpital du mali: À propos d’un cas. Annales d’Endocrinologie, 77, 454. https://doi.org/10.1016/j.ando.2016.07.595
[4]
Lanfranco, F., Kamischke, A., Zitzmann, M. and Nieschlag, E. (2004) Klinefelter’s syndrome. TheLancet, 364, 273-283. https://doi.org/10.1016/s0140-6736(04)16678-6
[5]
Chang, S., Skakkebæk, A., Trolle, C., Bojesen, A., Hertz, J.M., Cohen, A., et al. (2015) Anthropometry in Klinefelter Syndrome—Multifactorial Influences Due to CAG Length, Testosterone Treatment and Possibly Intrauterine Hypogonadism. TheJournalofClinicalEndocrinology&Metabolism, 100, E508-E517. https://doi.org/10.1210/jc.2014-2834
[6]
Groth, K.A., Skakkebæk, A., Høst, C., Gravholt, C.H. and Bojesen, A. (2013) Klinefelter Syndrome—A Clinical Update. TheJournalofClinicalEndocrinology&Metabolism, 98, 20-30. https://doi.org/10.1210/jc.2012-2382
[7]
O’Connor, M.J., Snyder, E.A. and Hayes, F.J. (2019) Klinefelter Syndrome and Diabetes. CurrentDiabetesReports, 19, Article No. 71. https://doi.org/10.1007/s11892-019-1197-3
[8]
Gravholt, C.H., Chang, S., Wallentin, M., Fedder, J., Moore, P. and Skakkebæk, A. (2018) Klinefelter Syndrome: Integrating Genetics, Neuropsychology, and Endocrinology. EndocrineReviews, 39, 389-423. https://doi.org/10.1210/er.2017-00212
[9]
Nielsen, J., Johansen, K. and Yde, H. (1969) Frequency of Diabetes Mellitus in Patients with Klinefelter’s Syndrome of Different Chromosome Constitutions and the XYY Syndrome. Plasma Insulin and Growth Hormone Level after a Glucose Load. TheJournalofClinicalEndocrinology&Metabolism, 29, 1062-1073. https://doi.org/10.1210/jcem-29-8-1062