2 results
21hydroxylasedeficiency diagram endocrinology fontan genetics procedure schematic
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics
Fontan Procedure Schematic A Fontan is done in most children (approximately 90%) who effectively have a single
valvular atresia or a congenital ... syndrome. ... Schematic #Diagram #congenital ... #Cardiology #Peds ... #Pediatrics #Pathophysiology
No results found for "Pediatrics peds syndrome symptoms cardiology physicalexam congenital constipation pathophysiology 21ohd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Pediatrics #peds #syndrome #symptoms #cardiology #physicalexam #congenital #constipation #pathophysiology #21ohd