Hyperkalaemic Ascending Paralysis
نویسندگان
چکیده
منابع مشابه
Post-operative hyperkalaemic paralysis.
Tetraparesis is more often a clinical feature of profound hypokalaemia 1, 2 than hyperkalaemia. Neurological features ofhyperkalaemia are rarely seen in clinical practice, as they are precluded by cardiotoxic complications such as arrhythmias. However, patients may develop flaccid paralysis of skeletal muscle with areflexia mimicking symptoms of acute inflammatory demyelinating polyneuropathy.3...
متن کاملHyperkalaemic paralysis due to spironolactone.
A case is reported of an adult who presented with hyperkalaemic muscular paralysis induced by spironolactone.
متن کاملSHORT REPORT Secondary hyperkalaemic paralysis
Besides the hereditary hyperkalaemic paralysis, a secondary form exists which often mimicks Guillain-Barre syndrome. A 62 year old patient is reported on who developed severe hyperkalaemic paralysis on the basis of mild renal failure and additive spironolactone intake. Neurophysiological examinations disclosed normal muscle fibre activity but delayed nerve conduction velocities indicating that ...
متن کاملAngiotensin converting enzyme inhibitor induced hyperkalaemic paralysis.
Secondary hyperkalaemic paralysis is a rare condition often mimicking the Guillain-Barré syndrome. There have been a few case reports of hyperkalaemia caused by renal failure, trauma, and drugs where the presentation has been with muscle weakness. A case of hyperkalaemic paralysis caused by an angiotensin converting enzyme inhibitor is reported.
متن کاملHyperkalaemic periodic paralysis: a rare presentation of Addison's disease.
A 44 year old man with longstanding diabetes mellitus gave a 6-month history of periodic attacks of flaccid quadriplegia. Following one of these episodes he was admitted for assessment. In view of persistent hyperkalaemia, hypoadrenalism was suspected and Addison's disease was confirmed biochemically. Adrenal replacement therapy restored the potassium levels to normal and resulted in no further...
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ژورنال
عنوان ژورنال: Journal of the Royal Society of Medicine
سال: 2004
ISSN: 0141-0768,1758-1095
DOI: 10.1177/014107680409700707