16 results
Kussmaul's Sign on Physical Exam

What’s the diagnosis?
Severe biventeicular failure with + Kussmaul sign! NICM. No constriction!

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inability of the right ... severe TR, RV infarct ... #physicalexam # ... clinical #video ... #jvp #cardiology
This chart shows the patterns of height (length) and weight for children from birth to 36
(length) and weight ... curved lines shows length ... Peds #Pediatrics #GrowthCharts ... #Infant #Weight ... #Height #Length
This chart shows the patterns of height (length) and weight for children from birth to 36
(length) and weight ... curved lines shows length ... Peds #Pediatrics #GrowthCharts ... #Infant #Weight ... #Height #Length
Severe Tricuspid Regurgitation on JVP Examination

What information about the patient do we get from this #JVP
Regurgitation on JVP ... Right-sided filling ... #TR #Lancisis #Sign ... #JVP #PhysicalExam ... #Clinical #Video
This chart shows the percentiles of length (height) for girls from birth to 36 months.
How to
percentiles of length ... from birth to 36 ... shows that at birth ... Diagnosis #Peds #GrowthCharts ... #Infant #Length
This chart shows the percentiles of length (height) for boys from birth to 36 months.
How to
percentiles of length ... from birth to 36 ... shows that at birth ... Diagnosis #Peds #GrowthCharts ... #Infant #Length
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... dehydration in an infant ... turgor Sudden weight ... Extremities #PhysicalExam ... #Signs #Symptoms
Kussmaul's Sign and Friedreich's Sign on Neck Examination

A middle-aged M with unknown PMH presents with dyspnea.
Kussmaul's Sign ... and Friedreich's Sign ... of screen) that might ... #PhysicalExam # ... Clinical #Video
Lancisi’s Sign in Severe Tricuspid Regurgitation

A 60-year-old man presented with progressive dyspnea and weight gain. A
Lancisi’s Sign in ... progressive dyspnea and weight ... Regurgitation #PhysicalExam ... #Clinical #Video ... Neck #Jugular #JVP
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... labeled as males at birth ... deficiencies present in infants ... Signs/Symptoms/Complications ... decr feeding, weight