16 results
Coins on Chest XRay - Trachea vs Esophagus

Coins in the sagittal plane on X-ray are more
plane on X-ray are ... Trachea #Esophagus #Peds ... #Pediatrics #CXR ... Radiology #Comparison #Clinical
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... , sleep apnea, cor ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Brudzinski’s Sign ... While the pathophysiology ... #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds
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Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... developmental age ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone
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Alzheimer’s Disease: Pathogenesis and Clinical Findings
Risk factor for Late Onset Alzheimer's (99% of cases):
 - Increasing
Pathogenesis and Clinical ... - Increasing age ... chromosome 21) Signs ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis
CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
Increased vital signs ... normal range for age ... in the ED, the clinician ... #Diagnosis #Peds ... #Pediatrics #PainScale
Tetralogy of Fallot - Chest XRay

An 18-month-old male presents with his parents who have noticed that
small for his age ... Fallot #ChestXRay #Clinical ... #Radiology #CXR ... #Peds #Pediatrics
Pediatric Elbow Injuries - Elbow Xrays

Check the fat pads on the lateral projection:
1. A displaced anterior
Pediatric Elbow ... fat pad (sail sign ... joint effusions are ... Xrays #Radiology #peds ... #Pediatrics #clinical
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection: 
 - Bacterial: Streptococcus
Pathogenesis and Clinical ... #OtitisMedia #pathophysiology ... diagnosis #symptoms #signs ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics