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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Materias: | |
| 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 |