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21hydroxylasedeficiency aorta chest disease endocrinology examination figure3 genetics incomplete kawasaki newborn pathophysiology physicalexam radiology sign xray
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 ... endocrinology #peds ... #pediatrics
Figure of 3 Sign - Coarctation of the Aorta on Chest X-Ray The figure of 3 sign
rib notching is caused ... seen in infancy ... Devpriyo Pal @drdevrad ... #Chest #XRay #clinical ... #radiology #pediatrics
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... if they have no clinical ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... When the diagnosis ... - reduced in coarctation ... #Examination #Peds ... #Pediatrics #Diagnosis
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