3 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... 21-OHase causes varying ... #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 ... Diagnosis #EM #Peds ... #Crying #Infant ... #Algorithm
Esophageal Variceal Bleeding - Scoping Summary
GENERAL PRINCIPLES OF MANAGEMENT (VARICEAL-B):
V - Vasoconstrictor therapy: (Octreotide 50mcg bolus
Variceal Bleeding - Scoping ... Summary GENERAL ... acquired/vasoactive meds ... Varices #Bleeding #Summary ... diagnosis #management #algorithm