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219 Possible Causes for Mild Facial Muscle Weakness, Muscular Atrophy

  • Peripheral Neuropathy

    Muscular atrophy of hand muscles persisted. Large fibers were involved more extensively than small fibers.[] The patient presented with mild facial weakness, humeral poly-hill sign, scapular winging, peroneal weakness, drop foot, pes cavus, and myoclonic epilepsy.[] Boulis works on novel treatments for several nerve disorders, including Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig's disease) and Spinal Muscular Atrophy[]

  • Muscular Dystrophy

    Distal muscular dystrophies are a group of inherited primary muscle disorders showing progressive weakness and atrophy preferentially in the hands, forearm, lower legs, or[] Mild involvement of the facial musculature (particularly of the orbicularis oculi and oris muscles) is often present.[] muscular dystrophy Spinal muscular atrophy (SMA) Myotonia congenita Myotonic dystrophy Charcot Marie Tooth disease (hereditary sensory motor neuropathy) At the Pediatric[]

  • Progressive Muscular Atrophy

    The name "spinal muscular atrophy" is ambiguous as it refers to any of various spinal muscular atrophies, including the autosomal recessive spinal muscular atrophy caused[] Experience mild weakness in their facial muscles. Weakness begins in the upper arm and lower leg muscles.[] KEYWORDS: Lower motor neuron syndrome; Lower motor neuron-onset ALS; PMA; Progressive muscular atrophy[]

  • Bell's Palsy

    atrophy : Werdnig-Hoffman disease - Kugelberg-Welander disease - Fazio Londe syndrome - MND ( Amyotrophic lateral sclerosis (ALS), Progressive muscular atrophy (PMA), Progressive[] It may be a year before the facial weakness has gone away completely. A few children may have mild, ongoing weakness in their facial muscles.[] muscles reduction or loss of taste sensation problems with dysarthria due to facial muscle weakness .[]

  • Primary Lateral Sclerosis

    This locus had not been implicated in ALS or in hereditary spastic parapareses, spinal muscular atrophy, or spinal and bulbar muscular atrophy. [7] A genetically mediated[] On examination, she had a spastic dysarthria with facial asymmetry. She had mild right-sided pyramidal distribution weakness.[] atrophy (PMA) and spinal muscular atrophies (SMAs) Upper and lower motor neurons - ALS ALS is the most common of the MNDs.[]

  • Amyotrophic Lateral Sclerosis

    Family history; fasciculations of facial muscles; gynaecomastia; proximal symmetrical weakness in addition to foot drop; mild sensory neuropathy on NCS; positive DNA test[] The patients were a 54-year-old man with progressive muscular atrophy who underwent removal of internal fixators in the arm and leg, and a 66-year-old woman with amyotrophic[] BACKGROUND: Informal caregivers of patients with Amyotrophic Lateral Sclerosis (ALS) or Progressive Muscular Atrophy (PMA) face stressful demands due to severe impairments[]

  • Polymyositis

    Kennedy disease or X-linked spinobulbar muscular atrophy is a rare X-linked recessive disorder with clinical features of slowly progressive atrophy and weakness of limb and[] Facial muscles are unaffected in PM and DM, but mild facial muscle weakness is common in patients with IBM.[] atrophy).[]

  • Charcot-Marie-Tooth Disease

    2015 ICD-9-CM Diagnosis Code 356.1 Peroneal muscular atrophy 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 356.1 is a billable medical code that[] At the age of 65, he was wheelchair-bound and had mild scoliosis, bilateral ophthalmoplegia, facial muscle weakness, inner ear hearing loss, distal-dominant weakness, and[] atrophy Peroneal muscular atrophy Charcot-Marie-Tooth disease、C-M-T[]

  • Erb Muscular Dystrophy

    At that time, the differentiation between the spinal muscular atrophies and weakness associated with central nervous system disorders and primary muscle disease had not been[] Affected individuals develop weakness of the lower limbs that may be mild or severe. Weakness of facial muscles may also occur.[] A heterogeneous group of genetic disorders characterized by progressive muscular atrophy and muscle weakness beginning in the hands, the legs, or the feet.[]

  • Chronic Inflammatory Demyelinating Polyneuropathy

    ., shoulders, elbows, hips, knees, ankles), clinodactyly, and evidence of mild but generalized muscle weakness.[] Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.[] Peroneal muscular atrophy (PMA) and related disorders: I.[]

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