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21hydroxylasedeficiency 21ohd cop cryptogenic fever genetics management organizing pathophysiology pediatrics pulmonary returning travel traveler tropical
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
be labeled as males ... Signs/Symptoms/Complications ... vomiting • Late (shock ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
decade of life, Males ... =Females SIGNS/ ... SYMPTOMS: • Acute ... misdiagnosed as CAP • Symptoms ... identified (autoimmune, meds
Fever in Returning Travelers from Tropical Regions - Frequent Differential Diagnoses Medical History: • Skin exposure to
Regions - Frequent Differential ... Diagnoses Medical ... without localizing signs ... rickettsioses, typhoid, measles ... Cough, dyspnea - Pneumonia
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