2 results
21hydroxylasedeficiency diagnosis endocrinology examination newborn pathophysiology physicalexam
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 ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... paediatrician or geneticist ... intra-abdominal masses ... #Examination #Peds ... #Pediatrics #Diagnosis
No results found for "rash nejm peds causes table adrenal criticalcare infant 21ohd pediatrics genetics"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #rash #nejm #peds #causes #table #adrenal #criticalcare #infant #21ohd #pediatrics #genetics