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pathophysiology peds 21hydroxylasedeficiency 21ohd diabetes diabeticketoacidosis diagnosis examination genetics infant newborn
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
out of cells may cause ... patient has good renal ... function/urine ... Signs/Symptoms/Complications ... pathophysiology #endocrinology
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 ... pathophysiology #genetics #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 ... of meningitis. ... are observed for signs ... Newborn #Infant #PhysicalExam ... Examination #Peds #Pediatrics
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