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peds diagnosis 21hydroxylasedeficiency age endocrinology examination genetics hypertension infant newborn pathophysiology physicalexam secondary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... also known as "congenital ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds #pediatrics
Age Distribution of Hypertension Etiologies < 1 month - Renal arterial thrombosis - Congenital renal disease -
thrombosis - Congenital ... Coarctation of the aorta ... #Hypertension #Causes ... Secondary #diagnosis #differential ... #age #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 ... intra-abdominal masses ... coarctation of the aorta ... Examination #Peds #Pediatrics
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