2 results
pediatrics 21hydroxylasedeficiency cirrhosis diagnosis endocrinology genetics hepatology liverfailure pathophysiology signs
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical Findings ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
#LiverFailure #Signs ... #Symptoms #PhysicalExam ... #Findings #Diagnosis ... #Peds #Pediatrics
No results found for "Overview peds pemsource physicalexam sign primitive symptoms findings 21ohd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Overview #peds #pemsource #physicalexam #sign #primitive #symptoms #findings #21ohd