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21hydroxylasedeficiency 21ohd examination newborn
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... deficiencies present in infants ... #genetics #endocrinology ... #peds #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
paediatrician or geneticist ... always needs urgent assessment ... #PhysicalExam # ... Examination #Peds ... #Pediatrics #Diagnosis
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