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diagnosis 21hydroxylasedeficiency abnormal cardiology chf cord criticalcare disorders endocrinology enzymes foamed genetics heartfailure hepatology icu lfts liver management neurology pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds #pediatrics
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
Cord Disorders - Differential ... neurological lesion: Clinical ... and signs below ... MCTD, Sjogren syndrome ... #algorithm
Abnormal liver function tests algorithm. This figure details the initial response to abnormal liver blood tests.
function tests algorithm ... symptoms/signs ... presence of metabolic syndrome ... LFTs #Abnormal #Algorithm ... Liver #Enzymes #Differential
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
Signs of congestion ... essentially Cardiogenic Shock ... acute coronary syndrome ... #diagnosis #differential ... #algorithm #management
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