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diagnosis pediatrics 21hydroxylasedeficiency algorithm endocrinology examination genetics management newborn pathophysiology physicalexam urinarytractinfection
Infant UTI Algorithm (<8 weeks of age) Emergency Medicine Cases @EMCases #Infant #Pediatric #UTI #Algorithm #Diagnosis #Management #UrinaryTractInfection
Infant UTI Algorithm ... Emergency Medicine Cases ... @EMCases #Infant ... #Pediatric #UTI ... UrinaryTractInfection #Peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... not present in infants ... #Newborn #Infant ... #Examination #Peds ... #Pediatrics #Diagnosis
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