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