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Spontaneous Sexual Development and Heavy Menstrual Bleeding in 45,X Monosomy and 45,X/47,XXX Mosaic Turner Syndrome and a Review of the Literature

Authors
Kim, Myeong JinJeong, Hwal Rim
Issue Date
Oct-2020
Publisher
Elsevier BV
Keywords
Turner syndrome; Menorrhagia; Spontaneous puberty
Citation
Journal of Pediatric and Adolescent Gynecology, v.33, no.5, pp 602 - 606
Pages
5
Journal Title
Journal of Pediatric and Adolescent Gynecology
Volume
33
Number
5
Start Page
602
End Page
606
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/2443
DOI
10.1016/j.jpag.2020.04.002
ISSN
1083-3188
1873-4332
Abstract
Turner syndrome (TS) is one of the most common sex chromosome disorders and is characterized by short stature and gonadal dysgenesis. A few patients with TS achieve normal sexual development, menarche, and even pregnancy. We encountered two cases of Turner syndrome with spontaneous sexual development and menstruation. The patients had different karyotypes, 45,X monosomy and 45,X/47,XXX mosaic TS, and presented with severe anemia due to excessive menstrual bleeding. Abnormal uterine bleeding patterns are expected in patients with primary ovarian insufficiency; however, the menstrual patterns of patients with TS have not been well described in the literature. Here, we describe these cases along with a brief review of the relevant literature.
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