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21hydroxylasedeficiency addisons adrenal diagnosis disease genetics insufficiency pathophysiology pediatrics peds primary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
disorder - Primary hypothyroidism ... Hypoparathyroidism - Type 1 diabetes ... Reduced libido • Signs ... addisons #disease #endocrinology ... #diagnosis #signs
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