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Approach to the Patient: The Adult With Congenital Adrenal Hyperplasia
The most common form of congenital adrenal hyperplasia is steroid 21-hydroxylase deficiency (21OHD). When the nonclassical (mild) form is included, 21OHD is the most common genetic disease in human beings. With the advent of pharmaceutical preparation of glucocorticoids starting in the 1960s and new...
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Main Authors: | , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Endocrine Society
2013
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3701266/ https://ncbi.nlm.nih.gov/pubmed/23837188 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2013-1440 |
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