19 results
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children

Urinary
Clinical Algorithm ... Evaluation and Management ... do not replace clinical ... #Peds #UrinaryTract ... #Pediatrics #Fever
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... Decreased level ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
Aortic Stenosis & Bicuspid Aortic Valve (AS)
 • Introduction & Pathophysiology
 • Classifications
 • Epidemiology
 •
Epidemiology • Clinical ... Radiologic/Diagnostic findings ... Pre-operative Management ... #AorticValve #cardiology ... #peds #pediatrics
Landolfi’s Sign on Physical Exam

A 73-year-old man presented with shortness of breath. On ocular exam, pupil
were noted, a finding ... severe aortic regurgitation ... present in this disease ... #PhysicalExam #Clinical ... AorticRegurgitation #Cardiology
Cardiac Amyloid - Diagnosis, Signs, Symptoms and Management

Clinical Presentation
- exertional dyspnea
- peripheral edema
- exertional syncope
- peripheral
, Symptoms and Management ... Clinical Presentation ... despite hx HTN) EKG Findings ... - conduction disease ... #Cardiology #Staging
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... Check for classic findings ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
Clinical features of Liver Disease in Children

#Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology

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Clinical features ... of Liver Disease ... #LiverFailure #Signs ... #PhysicalExam #Findings ... #Diagnosis #Peds
Plain radiography of the abdomen revealed calcification of both adrenal glands. A homozygous mutation in LIPA
deficiency, or Wolman’s disease ... accumulation in the liver ... #clincial #peds ... calcifications #infant ... NEJM #Wolmans #radiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Findings Autosomal ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Mucocutaneous Findings Kawasaki’s Disease - Patients present with diffuse red rash and fever with lymphadenopathy, strawberry
Mucocutaneous Findings ... Kawasaki’s Disease ... diffuse red rash and fever ... #Clinical #Peds ... #Pediatrics #Kawasaki