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54 Possible Causes for Hypomimia, Spastic Gait

Did you mean: hypomania, 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

    […] and hyperreflexia, and hemiplegic gait.[] ; Facial-faucial-finger mini-myoclonus (FFF); Spasticity; Mild paraparesis; Hyperreflexia; Extensor plantar responses; Pyramidal signs; Dementia; Generalized cerebral, cerebellar[] At age 10, he de- veloped spasticity of the lower limbs.[]

  • Autosomal Recessive Spastic Paraplegia Type 48

    […] recessive , and has symptoms including spastic paraplegia , urinary incontinence and spastic gait .[] He had cerebellar speech and hypomimia.[] If symptoms begin during the teenage years or later, then spastic gait disturbance usually progresses over many years.[]

  • 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.[] SPG4 is characterized by insidiously progressive bilateral lower-limb gait spasticity.[]

  • Wilson Disease

    […] present in various forms - tremor, akinesia, ataxia, dystonia with severe contractures and rigidity similar to Parkinson's disease, whereas spasticity, myoclonus, chorea, hypomimia[]

  • Infantile Dystonia - Parkinsonism

    She developed a mildly spastic gait at 10 years, which progressively worsened by age 13.[] We observed an increased tonus in the limbs, a bradykinesia and hypomimia.[] […] disturbance, limb spasticity, cerebellar signs, optic atrophy and confirmed by PLA2G6 gene.[]

  • Autosomal Dominant Spastic Paraplegia Type 31

    ; Spastic gait ; Spastic paraplegia ; Talipes equinovarus[] 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[]

  • Juvenile Paralysis Agitans of Hunt

    Mowing (Hemiplegic) Gait In spastic hemiplegia, as in unilateral extensor spasticity described above, there is a unilateral spastic gait in which the pelvis is tilted and[] Hypomimia- “masked facies”,expressionless face, blinking Speech abnormalities- Hypophonia: soft voice Aprosody of speech: monotonous and lack of inflection Tachyphemia: do[] The facial expression is markedly different from the hypomimia and masking of PD.[]

  • Niemann-Pick Disease Type D

    Older children are more likely to have problems with gait, balance, coordination, dystonia, spasticity, speech, swallowing and cognitive impairment, all of which worsen over[] There was slight hypomimia with a symmetrical slow smile. The remainder of his cranial nerves, including hearing, was intact.[]

  • Mitochondrial Membrane Protein-Associated Neurodegeneration

    [Thr11Met]þ[Gly69ArgfsX10] Initial symptoms Psychiatric Disturbance of visual acuity, spastic tetraparesis Gait impairment Pyramidal signs þþ þþþ – Dystonia þþ þ – Parkinsonism[] Hypomimia and bradykinesia were also noted. Eye fundus examination was normal.[] The most common symptoms are speech and gait difficulties, optic atrophy, generalized dystonia, spasticity and parkinsonism.[]

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