অক্ষমতা স্বেচ্ছাসেবী পেশী আন্দোলন তুল্য; নড়বড় আন্দোলন এবং টলটলায়মান গেইট

Noun:

অসমক্রিয়া, অপসংগতি,

ataxia শব্দের বাংলা অর্থ এর উদাহরণ:

অবশিষ্ট সায়ানাইড থেকে যাবে, তীব্র সায়ানাইড নেশা এবং গলগণ্ড, এবং এমনকি অপসংগতি বা আংশিক পক্ষাঘাতের কারণ হতে পারে. ।

ataxia's Usage Examples:

Friedreich's ataxia (FRDA or FA) is an autosomal-recessive genetic disease that causes difficulty walking, a loss of sensation in the arms and legs, and.

Spinocerebellar ataxia (SCA) is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition.

Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, is a rare, neurodegenerative, autosomal recessive.

Cerebellar ataxia is a form of ataxia originating in the cerebellum.

Non-progressive congenital ataxia (NPCA) is a classical presentation of cerebral ataxias.

Gluten ataxia accounts for 40% of ataxias of unknown origin and 15% of all ataxias.

Less than 10% of people with gluten ataxia present any gastrointestinal.

ATM since he found that its mutations are responsible for the disorder ataxia–telangiectasia.

Sensory ataxia is both a symptom and a sign in neurology.

It is a form of ataxia (loss of coordination) caused not by cerebellar dysfunction but by loss.

disorders, including familial hemiplegic migraine, episodic ataxia type 2, and spinocerebellar ataxia type 6.

Episodic ataxia (EA) is an autosomal dominant disorder characterized by sporadic bouts of ataxia (severe discoordination) with or without myokymia (continuous.

Symptoms include cerebellar ataxia, spasticity, optic atrophy, epilepsy, loss of motor functions, irritability.

including inherited and non-inherited forms of ataxia (such as the hereditary spinocerebellar ataxia known as Machado–Joseph disease) and multiple system.

"Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations".

anomalies and intellectual disability), or Gillespie syndrome (cerebellar ataxia).

spinocerebellar ataxia type 3 (SCA3), is a rare autosomal dominantly inherited neurodegenerative disease that causes progressive cerebellar ataxia, which results.

cerebellar degeneration which involves myoclonic epilepsy, progressive ataxia, tremor, and a dementing process.

ataxia's Meaning':

inability to coordinate voluntary muscle movements; unsteady movements and staggering gait