myasthenia$51116$ - traduction vers néerlandais
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myasthenia$51116$ - traduction vers néerlandais

HUMAN DISEASE
Myastenia gravis; Myasthenia Gravis; Mysathenia Gravis; Myasthenic crisis; Myasthenia gravis congenital; Juvenile myasthenia gravis; Congenital myasthenia gravis; Neonatal myathenia gravis; Erb-Goldflam syndrome; Myasthenia, familial; Neonatal myasthenia gravis
  • Azathioprine, chemical structure
  • Photograph of a person showing right partial ptosis (left picture), the left lid shows compensatory pseudo lid retraction because of equal innervation of the m. levator palpabrae superioris ([[Hering's law of equal innervation]]): Right picture: after an edrophonium test, note the improvement in ptosis.
  • Neostigmine, chemical structure
  • A chest CT-scan showing a thymoma (red circle)

myasthenia      
n. spierzwakte

Définition

myasthenia
[?m???s'?i:n??]
(also myasthenia gravis 'gr?:v?s, 'grav?s)
¦ noun a rare chronic autoimmune disease marked by muscular weakness without atrophy.
Origin
C19: mod. L., from Gk mus 'muscle' + asthenia.

Wikipédia

Myasthenia gravis

Myasthenia gravis (MG) is a long-term neuromuscular junction disease that leads to varying degrees of skeletal muscle weakness. The most commonly affected muscles are those of the eyes, face, and swallowing. It can result in double vision, drooping eyelids, trouble talking, and trouble walking. Onset can be sudden. Those affected often have a large thymus or develop a thymoma.

Myasthenia gravis is an autoimmune disease of the neuro-muscular junction which results from antibodies that block or destroy nicotinic acetylcholine receptors (AChR) at the junction between the nerve and muscle. This prevents nerve impulses from triggering muscle contractions. Most cases are due to immunoglobulin G1 (IgG1) and IgG3 antibodies that attack AChR in the postsynaptic membrane, causing complement-mediated damage and muscle weakness. Rarely, an inherited genetic defect in the neuromuscular junction results in a similar condition known as congenital myasthenia. Babies of mothers with myasthenia may have symptoms during their first few months of life, known as neonatal myasthenia. Diagnosis can be supported by blood tests for specific antibodies, the edrophonium test, or a nerve conduction study.

MG is generally treated with medications known as acetylcholinesterase inhibitors, such as neostigmine and pyridostigmine. Immunosuppressants, such as prednisone or azathioprine, may also be used. The surgical removal of the thymus may improve symptoms in certain cases. Plasmapheresis and high-dose intravenous immunoglobulin may be used during sudden flares of the condition. If the breathing muscles become significantly weak, mechanical ventilation may be required. Once intubated acetylcholinesterase inhibitors may be temporarily held to reduce airway secretions.

MG affects 50 to 200 per million people. It is newly diagnosed in three to 30 per million people each year. Diagnosis has become more common due to increased awareness. MG most commonly occurs in women under the age of 40 and in men over the age of 60. It is uncommon in children. With treatment, most of those affected lead relatively normal lives and have a normal life expectancy. The word is from the Greek mys, "muscle" and astheneia "weakness", and the Latin gravis, "serious".