Normal pathophysiology symptoms algorithm endocrinology adrenal workup injury peds crisis

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

• Salt wasting crisis ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics

$Scleroderma Renal Crisis (SRC) Clinical Presentation of Scleroderma Renal Crisis: 1) Acute kidney injury 2) Abrupt onset of hypertension 3)$

kidney injury ... hypertension 3) Abnormal ... anemia (MAHA) Pathophysiology ... endothelial cell injury ... , add other BP meds

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