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pediatrics 21hydroxylasedeficiency 21ohd dehydration diagnosis endocrinology examination newborn pathophysiology symptoms
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... #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
enzyme 21-OHase causes ... 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
is also a late sign ... paediatrician or geneticist ... #PhysicalExam # ... Examination #Peds ... #Pediatrics #Diagnosis
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