The 46, XX Ovotesticular Disorder of Sex Development With Xq27.1q27.2 Duplication Involving the SOX3 Gene: A Rare Case Report and Literature Review

Background: Very few reports are available on human XX ovotesticular disorder of sex development involving SOX3 gene duplication. Here we aim to present a rare case of SOX3 gene duplication in a person from the Chinese population who exhibits XX ovotesticular disorder of sex development. Case Presen...

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Dades bibliogràfiques
Publicat a:Front Pediatr
Autors principals: Zhuang, Jianlong, Chen, Chunnuan, Li, Jia, Jiang, Yuying, Wang, Junyu, Wang, Yuanbai, Zeng, Shuhong, Lin, Yiming, Xie, Yingjun
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2021
Matèries:
Pediatrics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8225946/
https://ncbi.nlm.nih.gov/pubmed/34178900
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2021.682846
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