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Hemiscrotal agenesis: a novel phenotype of a rare malformation
BACKGROUND: Hemiscrotal agenesis (HSA) is an exceedingly rare congenital anomaly in scrotal development. It is characterized by unilateral absence of scrotal skin with intact midline raphe. In the English literature, only seven patients were diagnosed with HSA. Herein, we report a 14-month-old boy w...
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| Yayımlandı: | BMC Pediatr |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7697378/ https://ncbi.nlm.nih.gov/pubmed/33248450 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-020-02424-y |
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