Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature

Author:

Maqdasy Salwan,Bogenmann Laura,Batisse-Lignier Marie,Roche Béatrice,Franck Fréderic,Desbiez Françoise,Tauveron Igor

Publisher

Springer Science and Business Media LLC

Subject

Developmental Biology,Endocrinology,Reproductive Medicine,Obstetrics and Gynecology

Reference111 articles.

1. Tartaglia N, Ayari N, Howell S, D’Epagnier C, Zeitler P. 48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome. Acta Paediatr Oslo Nor 1992. 2011;100:851–60.

2. Linden MG, Bender BG, Robinson A. Sex chromosome tetrasomy and pentasomy. Pediatrics. 1995;96(4 Pt 1):672–82.

3. Klinefelter HF, Reifenstein EC, Albright F. Syndrome characterized by gynecomastia, aspermatogenesis without A-Leydigism, and increased excretion of follicle-stimulating hormone1. J Clin Endocrinol Metab. 1942;2:615–27.

4. Fromantin M, Pesquies P, Serrurier B, Gautier D, Canivet B, Grenier J, et al. Klinefelter’s syndrome in 19 year old adolescents. (100 cases detected during selection for National Service). Ann Méd Interne. 1977;128:239–44.

5. Visootsak J, Ayari N, Howell S, Lazarus J, Tartaglia N. Timing of diagnosis of 47, XXY and 48, XXYY: A survey of parent experiences. Am J Med Genet A. 2013;161:268–72.

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