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61 Possible Causes for Hypomimia, Spastic Gait

  • Postencephalitic Parkinson Disease

    Symptoms and course Bradykinesia, rigidity, hypomimia, postural instability, gait disorders with falls and sialorrhea. Ophthalmoplegia and oculogyric crises.[] PARKINSON’S DISEASE Parkinson’s disease is characterized by a characteristic pill rolling tremor, bradykinesia, mask-like facies with a reduced blinking frequency (hypomimia[]

  • Pallidopyramidal Syndrome

    […] disorder characterized predominantly by spasticity and muscle weakness of the lower limbs, resulting in gait difficulties and loss of ambulation in some patients.[] Pill-rolling tremor, hypomimia, hypophonia, stooping posture, striatal toes and equinovarous deformity may be noted.[] ; Facial-faucial-finger mini-myoclonus (FFF); Spasticity; Mild paraparesis; Hyperreflexia; Extensor plantar responses; Pyramidal signs; Dementia; Generalized cerebral, cerebellar[]

  • Hereditary Spastic Paraplegia

    For many subjects with an ATL1 mutation, spastic gait begins in early childhood and does not significantly worsen, even over many years; such cases resemble spastic diplegic[] ., coarse features, bulbous nose and hypomimia); (c) developmental delay and intellectual disability; (d) early-onset spastic weakness of the lower limbs; and (e) cerebellar[] Characteristic clinical features comprise progressive spastic gait, cognitive impairment, and ataxia.[]

  • Autosomal Recessive Spastic Paraplegia Type 48

    If symptoms begin during the teenage years or later, then spastic gait disturbance usually progresses over many years.[] He had cerebellar speech and hypomimia.[] […] paraplegia (HSP) is heterogeneous group of genetically inherited disorders mainly characterized by spastic gait impairment.[]

  • Autosomal Recessive Spastic Paraplegia Type 49

    Walking pattern described as “spastic gait” occurs in which the following elements are present, each to variable degree in different individuals: a) heel strike is shifted[] Hereditary spastic paraplegia ( HSP ) is a group of inherited diseases whose main feature is a progressive gait disorder.[] Keywords Hereditary Spastic Paraplegia Spastic Paraparesis Primary Lateral Sclerosis Spastic Gait Hereditary Spastic Paraparesis These keywords were added by machine and not[]

  • Wilson Disease

    Spastic dystonia disorders manifest as mask-like facies, rigidity, and gait disturbance [ Svetel et al 2001 ].[] […] present in various forms - tremor, akinesia, ataxia, dystonia with severe contractures and rigidity similar to Parkinson's disease, whereas spasticity, myoclonus, chorea, hypomimia[]

  • Spinal Cord Tumor of Foramen Magnum

    The most common findings included hyperreflexia, arm or hand weakness, Babinski sign, spastic gait, sensory loss, and 11th cranial nerve involvement.[] Facial Expression: 0 — Normal. 1 — Minimal hypomimia, could be normal "poker face. ‎[] The most frequent presenting complaints were suboccipital neck pain, dysesthesias, gait disturbances, weakness, and hand clumsiness.[]

  • Progressive Supranuclear Palsy

    Neurological examination at age 67 disclosed pseudobulbar palsy, spastic gait, hyperreflexia, and presence of bilateral Hoffmann and Babinski signs.[] Examination shortly before death revealed hypomimia, dysarthria, vertical supranuclear gaze palsy and impaired postural reflexes.[] We report a 71-year-old woman with 15 years of seropositive rheumatoid arthritis who developed neurological complications: cognitive deterioration; hypomimia; limitation on[]

  • Paraparesis

    The aim of this study was to investigate the lower limb muscle coactivation and its relationship with muscles spasticity, gait performance, and metabolic cost in patients[] Facial Expression: 0 — Normal. 1 — Minimal hypomimia, could be normal "poker face. ‎[] If the patient can walk, look for a spastic gait with bilateral circumduction described as “scissoring”, and whilst they are standing inspect the spine for scars.[]

  • Autosomal Dominant Spastic Paraplegia Type 31

    Showing of 24 80%-99% of people have these symptoms Brisk reflexes 0001348 Proximal muscle weakness in lower limbs 0008994 Spastic gait Spastic walk 0002064 30%-79% of people[] Walking difficulties with imbalance, speech problems, and slowness, progressively stiff and he complained of leg weakness and falls, brisk reflexes, ankle clonus Facial hypomimia[] Children with very early onset may have relatively non-progressive spastic gait. 6 yrs, 2 – 50 yrs AD Uncomplicated/ Complicated Atlastin (SPG3A) DNA Sequencing Mainly pure[]

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