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Diagnostic and therapeutic considerations in Turner syndrome
Newly developed genetic techniques can reveal mosaicism in individuals diagnosed with monosomy X. Noninvasive prenatal diagnosis using maternal blood can detect most fetuses with X chromosome abnormalities. Low-dose and ultralow-dose estrogen replacement therapy can achieve a more physiological endo...
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| Publicado no: | Ann Pediatr Endocrinol Metab |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korean Society of Pediatric Endocrinology
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5769837/ https://ncbi.nlm.nih.gov/pubmed/29301182 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2017.22.4.226 |
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