অস্বাভাবিক দীর্ঘ পেশীবহুল সংকোচন; একটি সংকোচন পরে একটি পেশী ধীর শিথিলকরণ

myotonia's Usage Examples:

inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen).

of spontaneous release of the hands following strong handshakes due to myotonia (delayed relaxation of muscles after contraction) which accompanies muscle.

“paradoxical” myotonia.

This type of myotonia has been termed paradoxical because it becomes worse with exercise whereas classical myotonia, as seen in myotonia congenita.

Potassium-aggravated myotonia is a rare genetic disorder that affects skeletal muscle.

hyperkalemic periodic paralysis, paramyotonia congenita, and potassium-aggravated myotonia.

It is characterised by myotonia congenita, a hereditary condition which may cause it to stiffen or fall.

channel found in skeletal muscle, which is used to study animal models of myotonia congenita.

reduction of myotonia, improvement of circulation, and suppression of the pain reflex.

The drug inhibits the vicious circle of myotonia by decreasing.

hypokalemic (high and low potassium blood concentrations) periodic paralysis, myotonia congenita and paramyotonia congenita.

The two main types of myotonia congenita are Thomsen disease, which.

perlecan gene (HSPG2) which causes osteochondrodysplasia associated with myotonia.

Becker's muscular dystrophy (OMIM 300376) and Becker myotonia (OMIM 255700) are named after him.

from myotonic dystrophy (Steinert's disease) or nondystrophic myotonias such as myotonia congenita (Thomsen syndrome or Becker syndrome).

have resulted in weakness, headache, dizziness, nausea, abdominal pain, myotonia, hypotension, renal and hepatic injury, and delayed neuropathy.

one known hereditary genetic disorder found in the breed is congenital myotonia, a muscular condition also found in humans, dogs, cats, and goats.

sclerosis, amaurotic idiocy, paralysis agitans, Huntington’s chorea and myotonia congenita.

Mutations in CLCN1 lead to myotonia (OMIM: 160800), mutations in CLCN2 can lead to idiopathic generalised epilepsy.

rule out myotonia, or muscle stiffness that is detected by EMG.

Individuals with BD have stiff muscles but normal EMG results (pseudo-myotonia), where.

myotonia's Meaning':

abnormally long muscular contractions; slow relaxation of a muscle after a contraction

Synonyms:

tonicity; acromyotonia; tone; Thomsen's disease; tonus; myotonia congenita;

Antonyms:

atonicity; hypotonia; hypotonus; hypertonus; hypotonicity;