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46, XY complete gonadal dysgenesis with pubertal virilisation due to dysgerminoma/gonadoblastoma
Complete gonadal dysgenesis (CGD) or Swyer syndrome is characterised by sexual infantilism in a phenotypic female with 46, XY karyotype. Patients with gonadal dysgenesis and Y-chromosome material are at a high risk of developing gonadoblastoma and dysgerminoma. A 16-year-old girl presented with prog...
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| Gepubliceerd in: | BMJ Case Rep |
|---|---|
| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BMJ Publishing Group
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7342828/ https://ncbi.nlm.nih.gov/pubmed/32641439 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-235501 |
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