Cargando…
Potential risk of inguinal hernia in complete androgen insensitivity syndrome
Autores principales: | Kimizuka, Yu, Sato, Takeshi, Nakano, Satsuki, Ishii, Tomohiro, Hasegawa, Tomonobu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society for Pediatric Endocrinology
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887294/ https://www.ncbi.nlm.nih.gov/pubmed/36761490 http://dx.doi.org/10.1297/cpe.2022-0058 |
Ejemplares similares
-
A Novel Mutation of Androgen Receptor Gene in Complete Androgen Insensitivity
Syndrome
por: Narumi, Satoshi, et al.
Publicado: (2007) -
Complete androgen insensitivity syndrome with accelerated onset of puberty
due to a Sertoli cell tumor
por: Izawa, Masako, et al.
Publicado: (2021) -
Transient central diabetes insipidus after cranioplasty for craniosynostosis
in an infant with septo-optic dysplasia
por: Fukuyama, Takahiro, et al.
Publicado: (2021) -
Androgen Insensitivity Syndrome Diagnosed in an Elderly Patient During a Strangulated Inguinal Hernia Repair()()
por: Arslan, Yusuf, et al.
Publicado: (2013) -
Testosterone priming increased growth hormone peak levels in the stimulation
test and suppressed gonadotropin secretion in three Japanese adolescent
boys
por: Sato, Takeshi, et al.
Publicado: (2020)