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diagnosis 21hydroxylasedeficiency cardiology chf cord criticalcare csf disorders encephalitis endocrinology foamed genetics heartfailure icu management neurology pathophysiology pediatrics peds pharmacology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD
Summary of clinical findings for patients with encephalitis, by cause #Encephalitis #Signs #Symptoms #Table #Diagnosis #Differential #CSF
Summary of clinical ... encephalitis, by cause ... #Encephalitis #Signs ... #Symptoms #Table ... #Diagnosis #Differential
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 ... Non-compressive Spinal Cord Causes ... #algorithm
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
essentially Cardiogenic Shock ... the determined cause ... #diagnosis #differential ... #algorithm #management ... cardiology #treatment #table
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