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A novel pathogenic variant of SRD5A2 in an Iranian psuedohermaphrodite male
Deficiency of the 5‐alpha‐reductase may have an important role in 46,XY DSD in some cohorts. The prenatal ultrasonography and karyotyping can trigger the attention toward the presence of a DSD in fetus.
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| Publicado no: | Clin Case Rep |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7562857/ https://ncbi.nlm.nih.gov/pubmed/33088526 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3028 |
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