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diagnosis differential management 21hydroxylasedeficiency algorithm cardiology chf clinical criticalcare foamed genetics heartfailure hypertension icu indications pathophysiology pediatrics peds pharmacology sarcoidosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology
Causes of Secondary Hypertension - Workup and Differential Diagnosis Approach (when evaluation should be done): 1. Severe or
An acute rise or ... with previously stable ... hypertension and signs ... renal bruit or signs ... Vasculitis • Endocrinologic
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
are not caused ... Self-limiting, chronic but stable ... and progressive Acute ... : ACUTE, fever, ... Diagnosis #Management #Signs
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
important to recognize Acute ... essentially Cardiogenic Shock ... coronary syndrome ... the determined cause ... cardiology #treatment #table
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