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diagnosis management cardiology criticalcare treatment 21hydroxylasedeficiency 21ohd als amyotrophic chf clinica differential echocardiogram endocrinology genetics heartfailure icu lateral neurology pediatrics
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 ... endocrinology #peds
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
Signs of congestion ... essentially Cardiogenic Shock ... the determined cause ... #differential #algorithm ... treatment #table #foamed
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
combination of the clinical ... lateral sclerosis Pathophysiology ... in improperly folded ... - Causes progressive ... - Fatigue and decreased
Perhaps quite too often, the knee-jerk reaction to an elevated Troponin is to call our friends
heart (Sepsis, Shock ... treat the primary cause ... #diagnosis #algorithm ... echocardiogram #management #clinical ... #criticalcare #foamed
Perhaps quite too often, the knee-jerk reaction to an elevated Troponin is to call our friends
heart (Sepsis, Shock ... the only way to increase ... treat the primary cause ... management #cardiology #clinica ... l#foamed #algorithm
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