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pediatrics diagnosis 21hydroxylasedeficiency 21ohd clinical comatose examination genetics infant neurology 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 ... Signs/Symptoms/Complications ... non-arousable, decr urine ... #genetics #endocrinology ... #peds #pediatrics
Tone - Hand Position on Physical Exam A newborn baby’s hand is held in a fisted position
Tone - Hand Position ... will often cause ... is a sign of an ... #Hand #tone #Newborn ... #PhysicalExam #
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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 ... Muscle tone is assessed ... #PhysicalExam # ... Examination #Peds
The Neurological Evaluation of a Comatose Patient Definition: • Coma: a state of unresponsiveness; the absence of
• Mutism Pathophysiology ... • Vestibulo-ocular ... Motor/Sensory: • Tone ... • Examine for signs ... caseyalbin #PhysicalExam
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