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diagnosis pediatrics 21hydroxylasedeficiency 21ohd disease endocrinology evaluation incomplete kawasaki perioperative pfapa preop preoperative risk stratification syndrome
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
• This is also ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
old on day ≥7 of fever ... , elevation of ALT ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds
Preoperative Risk Evaluation Major Pre-Op Questions: 1. Does the patient have any modifiable risk factors that could be
or family - Ever ... event, follow ACC algorithm ... Cataract Plan for Meds ... are needed: • HgbA1c ... or death (CARP, DECREASE
PFAPA Syndrome - Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis EPIDEMIOLOGY: PFAPA is the most common syndrome entailing
(FMF) PATHOPHYSIOLOGY ... - Familial cold ... Also unlike PFAPA ... neutropenia (CyN) This genetic ... This drop can increase
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