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diagnosis pediatrics newborn physicalexam 21hydroxylasedeficiency abnormal breathing differential disease endocrinology examination floppy genetics hypotonic incomplete kawasaki pathophysiology patterns pulmonary
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 ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... #Causes #Peds #
Abnormalities in Rate and Rhythm of Breathing Normal The respiratory rate is about 14—20 per min
Abnormalities in ... 44 per min in infants ... punctuated by frequent sighs ... Occasional sighs ... narrowed airways increase
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... information about many abnormalities ... is also a late sign ... are observed for signs ... #Examination #Peds
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... purposes of this algorithm ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds
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