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diagnosis management 21hydroxylasedeficiency 21ohd antibiotics cryptogenic disease endocrinology febrile fever genetics incomplete infant kawasaki lp organizing pathophysiology pneumonia pulmonary risk
“Step by Step” – the new kid on the block – aims to risk stratify this
investigations and treatments ... components of the algorithm ... <10,000/mm3 - CRP ... Diagnosis #Management #Pediatrics ... #Peds #Febrile
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Males=Females SIGNS ... /SYMPTOMS: • Acute ... usually misdiagnosed as ... CAP • Symptoms ... , neoplastic) TREATMENT
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
occur in utero as ... Signs/Symptoms/Complications ... Labia major & minor ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
echo is positive, treatment ... clinical and lab signs ... (CRP, ESR) of ongoing ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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