Mayer-Rokitansky-Küster-Hauser syndrome with idiopathic central precocious puberty: a case report

BACKGROUND: Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is mainly characterized by congenital aplasia of the uterus and the upper two-thirds of the vagina in females with normal secondary sex characteristics and female karyotype (46,XX). MRKH syndrome is typically diagnosed due to primary amenorr...

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Detalles Bibliográficos
Autores principales: Jin, Wei, Gu, Chunjian, Fei, Zhenghua, Fei, Jingying, Wen, Gesheng, Min, Yanhua, Chen, Dongchan, Wu, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248929/
https://www.ncbi.nlm.nih.gov/pubmed/37305731
http://dx.doi.org/10.21037/tp-23-181

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248929/
https://www.ncbi.nlm.nih.gov/pubmed/37305731
http://dx.doi.org/10.21037/tp-23-181

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