Search results
Results from the WOW.Com Content Network
In electrocardiography, a strain pattern is a well-recognized marker for the presence of anatomic left ventricular hypertrophy (LVH) in the form of ST depression and T wave inversion on a resting ECG. [1] It is an abnormality of repolarization and it has been associated with an adverse prognosis in a variety heart disease patients.
S in V 1 + R in V 5 or V 6 (whichever is larger) ≥ 35 mm (≥ 7 large squares) R in aVL ≥ 11 mm; The Cornell voltage criteria [13] for the ECG diagnosis of LVH involve measurement of the sum of the R wave in lead aVL and the S wave in lead V 3. The Cornell criteria for LVH are: S in V 3 + R in aVL > 28 mm (men) S in V 3 + R in aVL > 20 mm ...
Small fiber peripheral neuropathy is a type of peripheral neuropathy that occurs from damage to the small unmyelinated and myelinated peripheral nerve fibers. These fibers, categorized as C fibers and small Aδ fibers, are present in skin, peripheral nerves, and organs. [1]
Meaning s̅: without (s with an overbar) (from Latin sine) S: sacrum: S x: symptoms surgery (though deemed by some as inappropriate) S 1: first heart sound: S 2: second heart sound: S 3: third heart sound S 4: fourth heart sound S&O: salpingo-oophorectomy Sb: Scholar batch SAAG: serum–ascites albumin gradient SAB: staphylococcal bacteremia
ultra: from Latin, meaning beyond; micro and scopic: from ancient Greek, meaning small looking, referring to the fineness of particulates; silico-: from Latin, silicon; volcano: from Latin, referring to volcano; coni: from ancient Greek (κόνις, kónis) which means dust-osis: from ancient Greek, suffix to indicate a medical condition
The American Heart Association's 2006 classification of cardiomyopathies considers noncompaction cardiomyopathy a genetic cardiomyopathy. [5] Mutations in LDB3 (also known as "Cypher/ZASP") have been described in patients with the condition. [6] There is recent information in which NCC has been seen in combination with 1q21.1 deletion Syndrome. [7]
Hereditary motor and sensory neuropathy are relatively common and are often inherited with other neuromuscular conditions, and these comorbidities cause an accelerated progression of the disease. [citation needed] Most forms of HMSN affect males earlier and more severely than females, but others show no predilection to either sex.
Peripheral neuropathy may be classified according to the number and distribution of nerves affected (mononeuropathy, mononeuritis multiplex, or polyneuropathy), the type of nerve fiber predominantly affected (motor, sensory, autonomic), or the process affecting the nerves; e.g., inflammation (), compression (compression neuropathy), chemotherapy (chemotherapy-induced peripheral neuropathy).