Doctor insights on:
How Fast Can I Make My Myopathy Go Away
I have a fast resting heart rate and low blood pressure. Does this mean my heart is not efficient? Could I have heart trouble valve or myopathy?
? POTS: Although there is very little other information, you could possibly have paroxysmal orthostatic tachycardia syndrome. The increase in heart rate would in particular occur upon standing. This can be accompanied by associated decrease in blood pressure - with lightheadedness, fatigue, excessive thirst. If chronic, can prompt cold extremities, shortness of breath, headache, restless sleep, GI symptom.
Need help husband has myopathy willing to go off all meds for reaserch&diagnosis we have kids&one of them already has signs help please?
Search for help: Last message lists research sites, but with the child having symptoms, sounds very likely of genetic origin, and this needs further assessment, again at a research facility. Include all children in such a study. Hang in there, many facilities have research and insights.See 1 more doctor answer
Myopathy: Myopathy is a muscle disorder. There are various causes and etiologies. Many times it mnay be from medication or from an auto-immune or rheuymatological condition. If the underlying condition is treated, the myopathy may improve.
Disease of muscle: By definition, this is a problem primarily associated with muscular damage and weakness. Classically, many of the disorders are hereditary, e.g., muscular dystrophy, but others may be autoimmune, such as polymyositis. The term implies focal involvement of muscle, as contrasted with neuropathy, which points to nerve problems.
Depends on cause: Typically muscle disease can be treated and controlled, but many forms are hereditary and resist current therapies. Some of the inflammatory and mitochondrial forms can be also challenging. This is a rather difficult area, which is being researched continuously. A good online source is the US Muscular Dystrophy Assoc (MDA).
Myopathy = muscle: Weakness & wasting from abnormal structure or metabolism of muscle cells. OMIM. Org lists 586 genetic defects that cause congenital myopathies. The many disorders that cause acquired myopathies are on clevelandclinicmeded. Com/medicalpubs/diseasemanagement/neurology/myopathy/. History, family history, physical & neurological exams, muscle biopsy, genetic & other lab studies are needed for diagnosis.
Many: Ck with isoenzymes, electrolytes, magnesium, calcium, serum myoglobins, serum creatinine, urinalysis, complete blood count, erythrocyte sedimentation test, thyroid function tests, ast, electrocardiograph, genetic testing, antinuclear antibodies, electromyogram, mri, muscle biopsy. As you can see there are many tests, but the most important thing is to select a physician that is a specialist.
Myopathy = muscle: Weakness & wasting from abnormal structure or metabolism of muscle cells. 586 specific genetic defects cause congenital myopathies. Causes of acquired myopathies are on clevelandclinicmeded. Com/medicalpubs/diseasemanagement/neurology/myopathy/. If personal & family history, physical & neurological exams, muscle biopsy & molecular genetic studies yield a diagnosis, your? Can be answered.
Myopathy: Myopathy means muscle pathology or disorder. There are many causes of muscle disease, i.e. Many muscle diseases. Whether or not medicine is needed depends on the specific muscle disease. Consider seeing a neurologist.
Depends on the level: At which its affected. The spinal cord lesion, say is at the C4 level, then the affected body part would be the shoulder and side of the neck. So if the lesion is at L3-4 level, then affected side's knee area would be affected. See a Spine surgeon to explain it to you, which particular site and the cause of the lesion responsible for it. Good Luck.See 1 more doctor answer
Hollow Visceral Myo-: Pathy = inability of intestinal smooth muscle to propel food, air & stool normally, causing obstruction without a lesion that blocks passage. It can be from inherited genetic defects affecting intestinal nerve & muscle cells, genetic syndromes or auto-immune & neurological diseases. Bladder function is often impaired, also. Biopsy of the walls of the bowel & bladder diagnose the type.
Muscle degeneration: There are several types of progressive muscle degeneration. Duchenne muscular dystrophy is one of the better known. Other variants of muscular dystrophy are less severe. Spinal muscular atrophy results from loss of anterior horn cells in the spinal cord that causes progressive degeneration of the involved muscles with weakness. Toxic myopathy can occur including associated with steroid use.
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