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newborn 21hydroxylasedeficiency clinical diagnosis endocrinology examination genetics hand pathophysiology tone video
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 ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... are observed for signs ... #PhysicalExam # ... Examination #Peds ... #Pediatrics #Diagnosis
Tone - Hand Position on Physical Exam A newborn baby’s hand is held in a fisted position
hand will often cause ... fisted hand is a sign ... neuron lesion in an infant ... clinical #video #peds ... #pediatrics
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