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21hydroxylasedeficiency algorithm bruising endocrinology examination facial genetics incomplete kawasaki pathophysiology physicalexam
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Facial bruising- Marked bruising of the face can occur during delivery. It is more common when
When the infant ... the body, the diagnosis ... #peds #pediatrics ... #clinical #photo ... facial #bruising #newborn
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... always needs urgent assessment ... #Newborn #Infant ... #Examination #Peds ... #Pediatrics #Diagnosis
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
incomplete Kawasaki Disease ... Infants ≤6 months ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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