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21hydroxylasedeficiency endocrinology examination hypertension infant newborn 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 ... Signs/Symptoms/Complications ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Age Distribution of Hypertension Etiologies < 1 month - Renal arterial thrombosis - Congenital renal disease -
- Mendelian genetic ... #Hypertension #Causes ... #differential # ... age #pediatrics ... #peds
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Birthweight, gestational age ... is also a late sign ... paediatrician or geneticist ... #Examination #Peds ... #Pediatrics #Diagnosis
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