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21hydroxylasedeficiency challenges criticalcare endocrinology genetics gout pathophysiology pediatrics responsiveness rheumatology tolerance treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
be labeled as males ... deficiencies present in infants ... Signs/Symptoms/Complications ... decr feeding, weight ... endocrinology #peds
Fluid Responsiveness and Fluid Tolerance Testing - OnePager Summary Fluid resuscitation can be beneficial when required or
with respiration might ... precede other signs ... #diagnosis #criticalcare ... #comparison #challenges ... #management
Gout - Diagnosis and Management Summary 3 Conditions for Gout to Manifest: 1. Hyperuricemia 2. Monosodium urate deposition in
and Management ... Advanced age • Male ... fingers Synovial Fluid ... Testing: • WBCs ... uricosuric) • Weight
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