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SAT-294 A Case of Turner Syndrome with Ambiguous Genitalia
Background: Turner syndrome is a common genetic condition caused by complete or partial absence of X chromosome. Often this condition is diagnosed prenatally. Neonates with this condition have variable presentations at birth, depending on the severity of genetic defect. Often these babies are born w...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Endocrine Society
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551818/ http://dx.doi.org/10.1210/js.2019-SAT-294 |