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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Detalles Bibliográficos
Autor principal: Yang, Seung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2017
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769837/
https://www.ncbi.nlm.nih.gov/pubmed/29301182
http://dx.doi.org/10.6065/apem.2017.22.4.226

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769837/
https://www.ncbi.nlm.nih.gov/pubmed/29301182
http://dx.doi.org/10.6065/apem.2017.22.4.226

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