Übersetzung für "Muskelerkrankung" in Englisch

You or your close family members have a hereditary muscle disorder

What does your doctor say about myopathy?

They say there's no myopathy.

Is a hereditary skin and muscle disease of young dogs.

Babies with this rare muscular disease might not survive the first few months of their lives.

This case report describes further ocular findings of this neuromuscular disorder.

The patient has an EMG or genetically confirmed muscular disease:

He was very sick, he had a severe muscular disorder and died at the age of 21.

This drug has been associated with a serious muscle condition known as rhabdomyolysis.

If a hereditary muscular disease is suspected in such patients, restarting Pravafenix therapy is not recommended.

Glybera must not be used in patients with immunodeficiency (weakened immunity), increased risk of bleeding and muscle disease.

Caution should be used in patients with predisposing factors such as renal impairment, hypothyroidism, previous history of muscular toxicity with a statin or fibrate, personal or familial history of hereditary muscular disorders, or alcohol abuse.

MAO-B inhibitors, or non-selective MAO-inhibitors) - have ever had neuroleptic malignant syndrome (NMS - this is a rare reaction to medicines used to treat severe mental disorders) - have ever had non-traumatic rhabdomyolysis (a rare muscle disorder) - have a severe liver disease.

If a patient has previously experienced a muscle disorder on a fibrate or a statin, treatment with a different member of the class should only be initiated with caution.

Rare side effects (may affect up to 1 in 1000 people) include lowering of normal body temperature; abnormal rhythms of the heart; sudden unexplained death;inflammation of the pancreas causing severe stomach pain, fever and sickness; liver disease appearing as yellowing of the skin and white parts of the eyes; muscle disease presenting as unexplained aches and pains; and prolonged and/or painful erection.

Muscle disease in JDM can be assessed by standardized muscle testing scores (childhood myositis assessment scale, CMAS; Manual Muscle Testing 8, MMT8) and blood tests (looking for elevated muscle enzymes and inflammation).

People with diabetes, underactive thyroid glands, kidney disease, or muscle disease sometimes need additional tests before or during atorvastatin therapy since dosage adjustments may be required.

Researchers from Berlin have discovered why cells from patients suffering from the rare muscular disease myotubular myopathy cannot function properly.

This form of non-inflammatory myopathy is a type of muscle disease caused by endocrine maladies such as hypo- and hyperthyroidism.

The reasons for that are not clear; some observers thought, that this behaviour was originated in the early death of his only legitimate son Alfredino, who had died of a muscle desease in 1956 in the age of only 24 years. Enzo Ferrari pretty often had forgiven von Trips a fauxpas concerning a lot of accidents happening at the beginning.

Other diseases or disorders that can be treated comprise: peripheral neuropathy, Alzheimer's disease, Parkinson's disease, Huntington's chorea or muscular atrophy, which e.g. result from denervation, chronic abuse, metabolic burden and malnutrition, or from a condition such as muscular dystrophy syndrome, congestive myopathy, an inflammatory muscular disease, toxic myopathy, nerve trauma, peripheral neuropathy, medicament- or toxin-induced damage or motoneuropathy.

Muscular Dystrophy is an inherited, progressive, and non-inflammatory degenerative muscular disease caused by a deficiency of dystrophyin, a muscle-membrane protein.

And, a tissue sample taken (biopsy) from the muscles behind the knees will be examined for muscle disease and/or nerve loss.

Noninflammatory metabolic myopathy is a rare muscle disease associated with metabolic disorders like various enzyme defects or storage of abnormal metabolic byproducts and others.