19 results
Cubital Tunnel Syndrome: Pathogenesis and clinical findings

 • Paresthesia of 5th and medial half of 4th
test • + Tinel sign ... • + Froment's sign ... + Wartenbergs sign ... #signs #symptoms ... #msk
Spondylolysis & Spondylolisthesis: Pathogenesis and Clinical Findings

Pars interarticularis stress fracture (spondylolysis) - most frequently in the
Pathogenesis and Clinical ... XR — scotty dog sign ... Spondylolisthesis #MSK ... #diagnosis #pathophysiology ... #signs #symptoms
McConnell's Sign on POCUS Echocardiogram - PSAX
Positive McConnell's Sign (hypokinetic RV with apical sparing) indicates acute
McConnell's Sign ... McConnell's Sign ... #McConnells #Sign ... #PSAX #clinical ... #cardiology #labeled
D-Sign in Pulmonary Embolism on POCUS Echocardiogram - PSAX

Pt having shortness of breath? POCUS can shed
D-Sign in Pulmonary ... Echocardiogram - PSAX ... light. ... D-sign = high RV ... #PSAX #clinical
Pulmonary Artery Clot seen on PSAX in Acute Saddle Pulmonary Embolism

Suspicious for PE? You can use
You can use #POCUS ... dilation, McConnell's sign ... Large clot in right ... Labeled Clip: https ... PulmonaryEmbolism #clinical
Pulmonary Artery Clot seen on PSAX in Acute Saddle Pulmonary Embolism - Labeled Thrombus in Purple

Suspicious
Clot seen on PSAX ... Embolism - Labeled ... dilation, McConnell's sign ... Large clot in right ... PulmonaryEmbolism #clinical
Uncommon Causes of Noncardiogenic Pulmonary Edema (NCPE) - Differential Diagnosis Framework

High Altitude Pulmonary Edema:
 • Accumulation
crackles in the right ... • Signs/Symptoms ... • Signs/Symptoms ... - The classic signs ... decreased respiratory rate
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
Cullen's sign. ... This sign is named ... Pathophysiology: ... It's typically a late ... onset of other symptoms
McConnell sign and right sided thrombus in transit on POCUS

Pt presents to highest acuity area of
McConnell sign and ... with McConnell sign ... Labeled Schematic ... #McConnell #sign ... #clinical
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Females may be labeled ... Signs/Symptoms/Complications ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology