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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.
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562857/ https://www.ncbi.nlm.nih.gov/pubmed/33088526 http://dx.doi.org/10.1002/ccr3.3028 |