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23 Possible Causes for Lower and Upper Limbs Affected, Muscular Fasciculation, Myoclonic Jerking

  • Amyotrophic Lateral Sclerosis

    […] atrophy weakness clinical fasciculations clumsiness Evaluation Diagnosis dependent on demonstration of both UMN and LMN involvement combination of UMN and LMN in the same[] Approximately 2/3 of patients with ALS show the spinal form of the disease (limb injuries) characterised by weakness and muscular loss in lower and upper limbs.[] Diseases that may mimic ALS include: Multifocal motor neuropathy, cervical myelopathy with radiculopathy, benign fasciculation syndrome, post-polio syndrome, spinobulbar muscular[]

  • Myoclonus-Dystonia Syndrome 11

    For instance, many people may occasionally experience a myoclonic jerk when falling asleep.[] Also in three of five affected family members, cardiac arrhythmias and attacks of painful cramps in upper and lower limbs were present ( 8 ).[] The upper extremities were usually more affected than the lower extremities. In one of these patients (nr. 4) there were perioral myoclonic jerks as well.[]

  • Myoclonic Jerking

    ., adj myoclon ic. A single myoclonic arm or leg jerk is normal when the person is falling asleep. Myoclonic jerks are severe with grand mal seizures.[] These twitches are considered harmless and are referred to as benign fasciculations.[] Attacks may last several minutes to half an hour and more frequently affect the lower than upper limbs.[]

  • Muscular Fasciculation

    jerks BFS symptoms are typically present when the muscle is at rest and are not accompanied by severe muscle weakness. [ citation needed ] In some BFS cases, fasciculations[] Register MUSCULAR FASCICULATION AND REACTIVE MYOTONIA IN POLYNEURITIS - 24 Hours access EUR 36.00 GBP 28.00 USD 45.00 Rental This article is also available for rental through[] Amyotrophic lateral sclerosis (ALS) both upper and lower motor neurones are affected limb muscle weakness and wasting ALS is the most common type, characterised by muscle[]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    Raymond et al (2008) noted that M-D due to SGCE mutations is characterized by early onset myoclonic jerks, often associated with dystonia.[] Type I spinal muscular atrophy (Werdnig-Hoffmann disease) is present in utero and becomes symptomatic by about age 6 mo.[] We examined a white Brazilian genealogy with 17 male patients who present a distal form of muscular atrophy affecting upper and lower limbs.[]

  • Essential Tremor

    jerks BFS symptoms are typically present when the muscle is at rest and are not accompanied by severe muscle weakness.[] In classic ET, 95% of patients have the upper limbs affected, the head in 34%, the lower limbs in 30%, the voice in 12%, the tongue, face, and trunk in only around 5%.[] Classic essential tremor most commonly affects the upper limbs, but it also can affect a patient’s head, lower limbs, voice, tongue, face, and trunk.[]

  • Myotonic Syndrome

    The muscular pain-fasciculation syndrome. Neurology. 1978 Nov. 28(11):1105-9. [Medline]. Isaacs H.[] jerks and other related symptoms.[] […] lastly the lower limbs were affected since 4 month.[]

  • Spinal Muscular Atrophy

    Here we report an adolescent female who presented with atonic and absence seizures and myoclonic jerks and was later diagnosed as having myoclonic-absence seizures.[] Extremities: Occasional tremors of fingers and muscular fasciculation may be observed in chronic infantile forms of SMA.[] The lower limbs usually are affected sooner and more profoundly than are the upper limbs.[]

  • Juvenile Paralysis Agitans of Hunt

    Hyperkinesias come in many forms, ranging from tremor to chorea to muscle fasciculations to myoclonic jerks.[] Psychosis Athetosis Choreoathetosis Clumsiness Foot dorsiflexor weakness EMG abnormality Paralysis Hypercholesterolemia Aspiration Poor head control Apathy Incoordination Spinal muscular[] affecting right nondominant side G83.14 Monoplegia of lower limb affecting left nondominant side G83.2 Monoplegia of upper limb Paralysis of upper limb Excludes1: monoplegia[]

  • Lower Motor Neuron Syndrome with Late-Adult Onset

    Subacute necrotizing encephalopathy, also called Leigh disease, is a lethal disorder of infancy marked by psychomotor delay, myoclonic jerks, paralyses of eye movements, and[] […] progressive, fasciculations, proximal weakness, resembles myopathy Anterior Horn Cell Disease -atrophy of pectoralis & thigh muscles Adult Onset Spinal Muscular Atrophy -[] Distal hereditary motor neuropathy affects nerve cells in the spinal cord and presents as weakness and wasting that starts in muscles of the upper and lower limbs and spreads[]