Defects+signs biceps symptoms pediatrics peds assessment painscale physicalexam findings signs

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11 results

Pediatric Cardiovascular Exam - Infographic Checklist

#PhysicalExam #Cardiovascular #Checklist #Cardiology #Signs #Findings #Peds #Pediatrics #Paediatrics

Pediatric Cardiovascular ... Infographic Checklist #PhysicalExam ... Checklist #Cardiology #Signs ... #Findings #Peds ... #Pediatrics #Paediatrics

The Febrile Child - some diagnostic clues to evaluating the febrile child.

#Febrile #Fever #Evaluation #Assessment #Signs

Fever #Evaluation #Assessment ... #Signs #Symptoms ... #PhysicalExam # ... Diagnosis #Peds ... #Pediatrics

Tetralogy of Fallot

1. Right ventricular outflow tract obstruction

2. Right ventricular hypertrophy

3. Ventricular septal

Ventricular septal defect ... Tetralogy #Fallot #Peds ... #Pediatrics #Cardiology ... #Signs #Symptoms

CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen

Increased vital signs ... #Diagnosis #Peds ... #Pediatrics #PainScale ... PostOperative #Assessment

Kawasaki Disease (Mucocutaneous Lymph Node Syndrome)
An rare systemic acute febrile vasculitic syndrome. Aetiology unknown.
Affects

Affects children ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics

Clinical features of shock from dehydration in an infant

Decreased level of consciousness
Sunken fontanelle
Dry mucous

Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics

#LiverFailure #Signs ... #Symptoms #PhysicalExam ... #Findings #Diagnosis ... #Peds #Pediatrics

Prader-Willi Syndrome: Pathogenesis and clinical findings
• Maternal uniparental disomy: inheriting 2 copies of maternal chromosome

Pathogenesis and clinical findings ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... pathophysiology #peds ... #pediatrics

Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection:
- Bacterial: Streptococcus

Pathogenesis and Clinical Findings ... 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 Findings ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics

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