Case Report: From epilepsy and uterus didelphys to Turner syndrome-associated dysgerminoma

Case Report: From epilepsy and uterus didelphys to Turner syndrome-associated dysgerminoma

Dysgerminoma is a rare occurrence in Turner syndrome patients without Y chromosome mosaicism or hormone therapy during puberty. We present a unique case of a 33-year-old nulliparous Chinese woman with intermittent epilepsy and Mullerian anomalies carrying a double uterus, cervix, and vagina. The pat...

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Bibliographic Details
Main Authors: Jinghua Li, Haipeng Zhu, Xuelian Ma, Jia Li, Jing Xue, Limin Feng
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-01-01
Series:Frontiers in Genetics
Subjects:
epilepsy
uterus didelphys
Turner syndrome
dysgerminoma
KIT mutation
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2023.1286515/full

Internet

https://www.frontiersin.org/articles/10.3389/fgene.2023.1286515/full

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