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physicalexam 21hydroxylasedeficiency 21ohd cirrhosis examination genetics hepatology infant liverfailure newborn pathophysiology symptoms
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
#LiverFailure #Signs ... #PhysicalExam #Findings ... #Diagnosis #Peds ... #Pediatrics #Hepatology ... GrepMed Recommended Text
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical Findings ... Females may be labeled ... 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 ... are observed for signs ... kidney on the left side ... #Examination #Peds ... #Pediatrics #Diagnosis
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