1 results
21hydroxylasedeficiency endocrinology genetics pathophysiology pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
No results found for "IntraAortic shock symptoms signs clinical personalitydisorder cardiology mnemonic peds 21ohd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #IntraAortic #shock #symptoms #signs #clinical #personalitydisorder #cardiology #mnemonic #peds #21ohd