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High 17-hydroxyprogesterone level in newborn screening test for congenital adrenal hyperplasia
We report a case of a female infant with an elevated 17-hydroxyprogesterone level detected in the newborn screening for 21-hydroxylase deficiency, the most common cause of congenital adrenal hyperplasia. The physical examination was unremarkable including no dysmorphism and no signs of virilisation....
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| Publicat a: | BMJ Case Rep |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4769481/ https://ncbi.nlm.nih.gov/pubmed/26912766 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2015-213939 |
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