Search results for "Congenital adrenal hyperplasia due to 21-hydroxylase deficiency"

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Reproductive Dysfunction in Classical and Nonclassical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

2021

Patients with congenital adrenal hyperplasia (CAH) both with severe (classical CAH) and mild (nonclassical NCAH) forms exhibit a wide spectrum of reproductive dysfunction. In this review, only CAH cases with 21-hydroxylase deficiency (21-OHd) will be discussed, as they represent almost all of the patients in reproductive clinical settings.

congenital hereditary and neonatal diseases and abnormalitiesmedicine.medical_specialtyendocrine system diseasesbiologybusiness.industry21-Hydroxylasenutritional and metabolic diseasesClinical settingsurologic and male genital diseasesmedicine.diseasefemale genital diseases and pregnancy complicationsCongenital adrenal hyperplasia due to 21-hydroxylase deficiencyEndocrinologyInternal medicinemedicinebiology.proteinCongenital adrenal hyperplasiabusiness
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