hypoglycemic pediatrics pathophysiology symptoms peds features physicalexam childhood alp 21ohd

Welcome to GrepMed! Sign up to bookmark, like, and share #FOAMed images to reach an audience of > 1 million weekly!

1 results

21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

Signs/Symptoms/Complications ... Hyperkalemia, Hypoglycemia ... #pathophysiology ... endocrinology #peds ... #pediatrics

No results found for "hypoglycemic pediatrics pathophysiology symptoms peds features physicalexam childhood alp 21ohd"
Try removing search terms or sorting by relevance

Or Upload an image for you and others searching for #hypoglycemic #pediatrics #pathophysiology #symptoms #peds #features #physicalexam #childhood #alp #21ohd

No results found for "hypoglycemic pediatrics pathophysiology symptoms peds features physicalexam childhood alp 21ohd" Try removing search terms or sorting by relevance

No results found for "hypoglycemic pediatrics pathophysiology symptoms peds features physicalexam childhood alp 21ohd"
Try removing search terms or sorting by relevance