
Sturge-Weber syndrome
Sturge-Weber syndrome (SWS) is a rare, congenital neurocutaneous disorder characterised by capillary-venous malformations involving the skin, leptomeninges, and ocular structures.
Sturge-Weber syndrome (SWS) is a rare, congenital neurocutaneous disorder characterised by capillary-venous malformations involving the skin, leptomeninges, and ocular structures.
62 year-old woman with two hours of central crushing chest pain. Smoker, hypertension. ETA 30 minutes.
Emergency Procedure: Radial Arterial Line, with a guide made in partnership with a recent publication in Emergency medicine Australasia
45 year-old man with two hours of central chest pain. Smoker, significant family history of IHD. ETA 20 minutes.
86 year-old woman with two hours of dull chest pain and dizziness. Ex-smoker with hypertension and dyslipidaemia. ETA 20 minutes.
58 year-old man with one week of pleuritic chest pain and SOB. Background of previous pericarditis. ETA 30 minutes.
Carl Wernicke (1848–1905), German neurologist who described Wernicke’s area and aphasia, and identified Wernicke’s encephalopathy from thiamine deficiency
30-year-old male presents following a work place injury. A 20cm metal rod has fallen on his face, resulting in a penetrating orbital injury.
Further reading
Lower brachial plexus injury, with consequent weakness and wasting of the C8–T1 musculature. Augusta Klumpke (1859-1927)
46-year-old male with one hour of central crushing chest pain. Background of hypertension, morbidly obese and a heavy smoker.
A 66-year-old lady presents with left sided facial droop and hemiparesis, headache and vomiting. A CT stroke series is performed