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21hydroxylasedeficiency crisis diagnosis genetics management pediatrics renal rheumatology scleroderma src
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... #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)
) Acute kidney injury ... anemia (MAHA) Pathophysiology ... , add other BP meds ... • Refractory cases ... #rheumatology #nephrology
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