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21hydroxylasedeficiency dehydration diagnosis endocrinology examination newborn pathophysiology pediatric shock supraventricular svt tachycardia treatment
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
dehydration in an infant ... Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... rate changes • Infants ... Signs of shock or ... #Algorithm #peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... 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 ... are observed for signs ... #PhysicalExam # ... Examination #Peds ... #Pediatrics #Diagnosis
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