3 results
physicalexam 21hydroxylasedeficiency 21ohd diagnosis endocrinology examination newborn pathophysiology signs
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
from dehydration ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Infant #Dehydration ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... pathophysiology #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 ... for any midline defects ... #Examination #Peds ... #Pediatrics #Diagnosis
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