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pathophysiology pediatrics peds 21hydroxylasedeficiency clinical crypto cryptococcal diabetes diabeticketoacidosis diagnosis dka examination genetics infant mri newborn radiology t2
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 ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings • Note: in DKA, body K+ is lost
out of cells may cause ... renal function/urine ... be used by the brain ... Signs/Symptoms/Complications ... pathophysiology #endocrinology
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
surrogate measure of brain ... is also a late sign ... of meningitis. ... are observed for signs ... Newborn #Infant #PhysicalExam
Cryptococcal meningitis on T2 MRI 30 M from sub-Saharan Africa presents w/ progressive Headache x1 mo, +neck
Cryptococcal meningitis ... organism (soap bubble sign ... Nausea & vomiting ... of K+ & Mg in urine ... #T2 #MRI #Brain
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