Carriers of 21-hydroxylase deficiency are not at increased risk for hyperandrogenism

Medicine & Life Sciences

• Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 100%
• Hyperandrogenism 93%
• Mutation 39%
• Androgens 36%
• Dehydroepiandrosterone Sulfate 25%
• Adrenocorticotropic Hormone 19%
• Hyperplasia 17%
• Cosyntropin 14%
• 17-alpha-Hydroxyprogesterone 14%
• Gene Conversion 13%
• Congenital Adrenal Hyperplasia 13%
• Hirsutism 13%
• Sex Hormone-Binding Globulin 12%
• Androstenedione 12%
• Population 11%
• Heterozygote 10%
• Menstrual Cycle 10%
• Parity 10%
• Inborn Genetic Diseases 9%
• Testosterone 8%
• Mothers 6%
• Weights and Measures 6%
• Phenotype 6%
• Confidence Intervals 6%

Chemical Compounds

• Mutation 59%
• Androgen 50%
• Dehydroepiandrosterone Sulfate 32%
• Testosterone 11%
• Disorder 8%