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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....
Gorde:
| Argitaratua izan da: | BMJ Case Rep |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BMJ Publishing Group
2016
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| Gaiak: | |
| Sarrera elektronikoa: | 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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