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21hydroxylasedeficiency 21ohd clinical cullen diagnosis em emergencymedicine endocrinology endoscopy esophageal fm genetics im image management mnemonic pancreatitis pediatrics peritonitis surgery
Esophageal Variceal Bleeding - Scoping Summary GENERAL PRINCIPLES OF MANAGEMENT (VARICEAL-B): V - Vasoconstrictor therapy: (Octreotide 50mcg bolus
- Scoping Summary ... acquired/vasoactive meds ... Hgb>7gm/dL) I - ICU ... #Summary #Endoscopy ... diagnosis #management #algorithm
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
Pathophysiology: ... It's typically a late ... In summary, Cullen's ... #cullensign #em ... peritonitis #IM #FM #ICU
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
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