1 results
21hydroxylasedeficiency pediatrics peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
congenital adrenal hyperplasia ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
No results found for "msk pathophysiology pharmacology symptoms neurology hyperplasia endocrinology genetics 21ohd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #msk #pathophysiology #pharmacology #symptoms #neurology #hyperplasia #endocrinology #genetics #21ohd