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An acute, fulminating, potentially fatal disease of skeletal muscle that entails destruction of muscle, as evidenced by myoglobinemia and myoglobinuria. [rhabdo- + G. mys, muscle, + lysis, loosening]
- acute recurrent r. [MIM*268200] repeated paroxysmal attacks of muscle pain and weakness followed by passage of dark red-brown urine, often precipitated by intercurrent illness and diagnosed by demonstration of myoglobin in the urine; it is attributed to abnormal phosphorylase activity in skeletal muscle, but there may be more than one biologic type; probably autosomal recessive inheritance. In some cases, at least, there is deficiency of carnitine palmitoyl transferase. SYN: familial paroxysmal r..
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rhab·do·my·ol·y·sis .rab-dō-mī-'äl-ə-səs n, pl -y·ses -.sēz the destruction or degeneration of skeletal muscle tissue (as from traumatic injury, excessive exertion, or stroke) that is accompanied by the release of muscle cell contents (as myoglobin and potassium) into the bloodstream resulting in hypovolemia, hyperkalemia, and sometimes acute renal failure
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rhab·do·my·ol·y·sis (rab″do-mi-olґĭ-sis) [rhabdo- + myo- + -lysis] disintegration or dissolution of muscle, associated with excretion of myoglobin in the urine.Medical dictionary. 2011.