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physicalexam 21hydroxylasedeficiency 21ohd birthweight dehydration diagnosis endocrinology examination genetics low newborn pathophysiology premature presentation problems shock
Summary of problems of Very Low Birthweight Infants #Premature #Low #Birthweight #Peds #Pediatrics #Problems #Signs #Symptoms #Presentation
Low Birthweight Infants ... #Birthweight #Peds ... #Pediatrics #Problems ... #Signs #Symptoms
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
dehydration in an infant ... #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
deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
pressure and cranial ultrasound ... is also a late sign ... are observed for signs ... #Examination #Peds ... #Pediatrics #Diagnosis
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