12 results
CT Lung Signs in Pulmonary Diseases - One Page Summary of Pulmonary Signs
 - Air Crescent
CT Lung Signs in ... Pulmonary Diseases ... - One Page Summary ... of Pulmonary Signs ... Lung #Signs #Pulmonary
Summary of problems of Very Low Birthweight Infants

#Premature #Low #Birthweight #Peds #Pediatrics #Problems #Signs #Symptoms #Presentation
Summary of problems ... #Birthweight #Peds ... #Pediatrics #Problems ... #Signs #Symptoms
Total Anomalous Pulmonary Venous Return (TAPVR)
 • Introduction
 • Classification
 • Pathophysiology of TAPVR
 • Presentation
Total Anomalous Pulmonary ... Classic “snowman sign ... Total #Anomalous #Pulmonary ... management #cardiology #peds ... #pediatrics #summary
Signs and Symptoms of Respiratory Distress Through the Years. 

#signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... differential #neonatal #pediatrics ... #adult #peds #pulmonary
Standardized Physical Abuse Guideline
<6 months of age
 • Social work consult
 • Skeletal survey
 • Head
survey • Head CT ... • Abdominal CT ... AST or ALT> 80, signs ... Guidelines #Workup #Peds ... #Pediatrics #Diagnosis
PECARN Head CT Decision Aid

The Head CT Choice decision aid was developed in Rochester, Minnesota. Full
PECARN Head CT Decision ... Aid The Head CT ... observation, and signs ... #PatientInfo #Peds ... #Pediatrics #DecisionAid
Paradoxical Breathing on Physical Exam

Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... clinical #video #pulmonary ... #peds #pediatrics
Pott's Disease in Tuberculosis - Diagnosis and Management Summary
Epidemiology:
 - Typically from TB endemic areas
 -
and Management Summary ... cases Clinical Signs ... years - May have signs ... symptoms of active pulmonary ... involvement - CT
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... sleep apnea, cor pulmonale ... pathophysiology #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 ... pathophysiology #genetics #endocrinology ... #peds #pediatrics