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signs clinical genetics newborn pathophysiology 21hydroxylasedeficiency 21ohd birthweight cardiology cyanosis dehydration diagnosis endocrinology fallot low perioral physicalexam praderwilli premature presentation
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
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
This is part of acrocyanosis ... The skin in this infant ... #clinical #photo ... #peds #pediatrics ... perioral #cyanosis #acrocyanosis
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
Acrocyanosis- As this infant is transitioning, the blue color on the feet is starting to resolve
Acrocyanosis- As ... this infant is ... #clinical #photo ... #peds #pediatrics ... #newborn #acrocyanosis
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... , sleep apnea, cor ... pathophysiology #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
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