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diagnosis pediatrics 21hydroxylasedeficiency em endocrinology examination genetics newborn pathophysiology
Algorithm for the evaluation of the crying infant #Diagnosis #EM #Peds #Crying #Infant #Algorithm
Algorithm for the ... evaluation of the crying ... infant #Diagnosis ... #EM #Peds #Crying ... #Infant #Algorithm
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... 21-OHase causes varying ... deficiencies present in infants ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... the baby is not crying ... the heart, the normal ... #PhysicalExam # ... Examination #Peds
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