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pediatrics 21hydroxylasedeficiency 21ohd clinical diagnosis endocrinology examination genetics hand 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 ... non-arousable, decr urine ... endocrinology #peds
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 ... #PhysicalExam # ... clinical #video #peds
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 Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... is also a late sign ... #Newborn #Infant ... #PhysicalExam # ... Examination #Peds
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