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diagnosis 21hydroxylasedeficiency 21ohd classification differential examination genetics newborn pathophysiology physicalexam rheumatology vasculitides vasculitis
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 ... 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 ... Any intra-abdominal ... usually renal in ... #Examination #Peds ... #Pediatrics #Diagnosis
Vasculitis and Vasculitides - Differential Diagnosis Framework When to Consider Vasculitis: • Purpura, ischemic skin lesions •
tract, and often causes ... - GI tract: abdominal ... mucositis - Rash ... purpura: strong sign ... pain, infarct
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