44 results
diagnosis sign ophthalmology urology management abdominal msk neck stone cholelithiasis gallbladder papilledema transverse acute anatomy artery ascites central crao disease
Central retinal artery occlusion (CRAO). Positive "spot sign" on Ocular Ultrasound 78 yo M with sudden onset
Positive "spot sign ... " on Ocular Ultrasound ... Occlusion #Embolus #Clinical ... #POCUS #Ocular ... #Ultrasound
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 Seagull Sign on POCUS - Celiac Artery Trunk Anatomy Celiac trunk branching into hepatic and splenic arteries
Seagull Sign on ... NephroP #Seagull #Sign ... Artery #Trunk #labeled ... #clinical #pocus ... #ultrasound #transverse
Spondylolysis & Spondylolisthesis: Pathogenesis and Clinical Findings Pars interarticularis stress fracture (spondylolysis) - most frequently in the
Pathogenesis and Clinical ... XR — scotty dog sign ... vertebrae • CT - collar ... MSK #diagnosis #pathophysiology ... #signs #symptoms
Hemothorax on Lung POCUS with Spine Sign GSW to left chest. Perisplenic window focusing on lower
Hemothorax on Lung POCUS ... with Spine Sign ... Labeled Schematic ... #Spine #Sign #clinical ... #ultrasound #Pulmonary
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 Stone-In-Neck Sign on Gallbladder POCUS This 40yo F presented with R flank pain. Here is her biliary
Stone-In-Neck Sign ... sign). ... #Sign #POCUS #clinical ... #gallbladder #ultrasound ... #abdominal #labeled
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 Severe Hydronephrosis on POCUS Based on this clip, which of the following is most likely abnormal? Resolution: creatinine
can be elevated in ... Labeled Schematic ... #Severe #Clinical ... #Ultrasound #Renal ... #Nephrology
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 Papilledema on Ocular POCUS Eye, linear probe, optic nerve (ON) elevation >0.6 mm into globe (crescent sign)
Papilledema on Ocular ... globe (crescent sign ... #POCUS #clinical ... #ultrasound #ophthalmology ... #labeled
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 Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
and Clinical Findings ... areas → Errors in ... #diagnosis #signs ... #symptoms #Brocas ... #Wernickes #neurology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... recessive mutation in ... Females may be labeled ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology
Ureteral Stone on Renal POCUS A 23yo male with no significant PMHx presents with acute LLQ pain,
Stone on Renal POCUS ... DC home (w/ op urology ... rupture—not uncommon in ... controlled, & no signs ... #clinical #ultrasound
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