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Stokes–Adams disease : ウィキペディア英語版 | Adams–Stokes syndrome
Stokes–Adams syndrome (alternative eponyms include Gerbezius-Morgagni-Adams–Stokes syndrome and Gerbec-Morgagni-Adams–Stokes syndrome) refers to a sudden, transient episode of syncope, occasionally featuring seizures. Named after two Irish physicians, Robert Adams (1791–1875)〔R. Adams. Cases of Diseases of the Heart, Accompanied with Pathological Observations. Dublin Hospital Reports, 1827, 4: 353–453.〕 and William Stokes (1804–1877),〔W. Stokes. Observations on some cases of permanently slow pulse. Dublin Quarterly Journal of Medical Science, 1846, 2: 73–85.〕 the first description of the syndrome was published in 1717 by the Carniolan physician of Slovene descent Marko Gerbec, which was 44 years after its publication quoted by Giovanni Battista Morgagni. ==Signs and symptoms== Prior to an attack, a patient may become pale, their heart rhythm experiences a temporary pause, and collapse may follow. Normal periods of unconsciousness last approximately thirty seconds; if seizures are present, they will consist of twitching after 15–20 seconds. Breathing continues normally throughout the attack, and so on recovery the patient becomes flushed as the heart rapidly pumps the oxygenated blood from the pulmonary beds into a systemic circulation which has become dilated due to hypoxia. As with any syncopal episode that results from a cardiac dysrhythmia, the faints do not depend on the patient's position. If they occur during sleep, the presenting symptom may simply be feeling hot and flushed on waking.〔
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