A patient with 47, XYY mosaic karyotype and congenital absence of bilateral vas deferens: a case report and literature review

BACKGROUND: The incidence of 47, XYY syndrome in live-born male infants is 1/1000. Due to its variable clinical symptoms, the diagnosis is easy to miss. The incidence of congenital bilateral absence of the vas deferens (CBAVD) in infertile men is 1–2%. The main cause is the mutation of CFTR and ADGA...

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Detalles Bibliográficos
Autores principales: Zou, Ci, Yu, Dexin, Geng, Hao, Lan, Xiaofeng, Sun, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809031/
https://www.ncbi.nlm.nih.gov/pubmed/35109852
http://dx.doi.org/10.1186/s12894-022-00965-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809031/
https://www.ncbi.nlm.nih.gov/pubmed/35109852
http://dx.doi.org/10.1186/s12894-022-00965-1

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