Two Cousins with 17-Alpha Hydroxylase Deficiency - Case Report
Abstract We present two cases of 17-alpha hydroxylase deficiency (17OHD), a rare cause of congenital adrenal hyperplasia (1%); our patients are first cousins (their fathers are brothers). Genetically female patients with congenital adrenal hyperplasia due to 17OHD represent with sexual infantilism...
Bewaard in:
| Hoofdauteurs: | , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Society of Endocrinology and Metabolism of Turkey
2010-09-01
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| Reeks: | Endocrinology Research and Practice |
| Onderwerpen: | |
| Online toegang: | https://www.endocrinolrespract.org/index.php/pub/article/view/566 |
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