10 results
Lancisi's sign in Severe Tricuspid Regurgitation - Physical Exam
Note the large systolic jugular venous wave caused
Lancisi's sign in ... #Lancisis #sign ... #PhysicalExam #Cardiology ... #Neck #Jugular ... #JVP
Lancisi’s Sign in Severe Tricuspid Regurgitation

A 60-year-old man presented with progressive dyspnea and weight gain. A
Lancisi’s Sign in ... known as Lancisi’s sign ... Lancisi’s sign is ... #Lancisis #Sign ... #Jugular #JVP #
Lancisi's Sign on Neck Examination in Severe Tricuspid Regurgitation

Semiology of severe tricuspid insufficiency : venous pulse
Lancisi's Sign on ... Neck Examination ... v wave of the jugular ... #Lancisis #Sign ... #Neck #JVP #Clinical
Lancisi’s Sign in Severe Tricuspid Regurgitation 

- Reza Karimianpour, D.O. @officialdrk12

#Lancisis #Sign #Tricuspid #Regurgitation #PhysicalExam #Clinical
Lancisi’s Sign in ... #Lancisis #Sign ... Clinical #Video #Neck ... #Jugular #JVP # ... Cardiology
Lancisi's Sign - Severe Trisuspid Regurgitation on neck JVP examination.

What's the valvular lesion? 

Those are giant
Lancisi's Sign - ... on neck JVP examination ... #Lancisis #Sign ... #Jugular #JVP # ... Cardiology
Lancisi's Sign - Severe Trisuspid Regurgitation on neck JVP examination.

What's the valvular lesion?  Here's the
Lancisi's Sign - ... on neck JVP examination ... #Lancisis #Sign ... #Jugular #JVP # ... Cardiology
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 ... PraderWilli #Syndrome #genetics ... pathophysiology #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 ... radial head and neck ... Injuries #Xrays #Radiology ... #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