2 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHase causes varying ... Enlarged clitoris may look ... minor fuse to look ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Algorithm for the evaluation of the crying infant #Diagnosis #EM #Peds #Crying #Infant #Algorithm
Algorithm for the ... evaluation of the crying ... infant #Diagnosis #EM ... #Peds #Crying # ... Infant #Algorithm