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peds diagnosis infant 21hydroxylasedeficiency assessment dehydration endocrinology examination febrile fever genetics pathophysiology
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
diagnostic clues to evaluating ... Febrile #Fever #Evaluation ... #Assessment #Signs ... #Symptoms #PhysicalExam ... Diagnosis #Peds #Pediatrics
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features of shock ... Extremities #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 ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... is also a late sign ... requires further evaluation ... #PhysicalExam # ... Examination #Peds #Pediatrics
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