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A novel mutation in CYP17A1 gene leads to congenital adrenal hyperplasia: A case report
BACKGROUND: Congenital adrenal hyperplasia is a rare autosomal recessive disorder where the mutation in P450 family 17 subfamily A member 1 gene (CYP17A1) is involved in its etiology. The disorder represents itself with low blood levels of estrogens, androgens, and cortisol that generally couples wi...
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| Udgivet i: | Int J Reprod Biomed |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Knowledge E
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6719517/ https://ncbi.nlm.nih.gov/pubmed/31508570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18502/ijrm.v17i6.4817 |
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