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58 Possible Causes for Hypomimia, Spastic Gait

Did you mean: hypoxemia, spastic gait

  • Postencephalitic Parkinson Disease

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

  • Pallidopyramidal Syndrome

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

  • Hereditary Spastic Paraplegia

    Initial symptoms that make be experienced are mild difficulties in walking style (causing what is called a spastic gait) and mild leg stiffness.[mda.org.nz] ., coarse features, bulbous nose and hypomimia); (c) developmental delay and intellectual disability; (d) early-onset spastic weakness of the lower limbs; and (e) cerebellar[ncbi.nlm.nih.gov] […] and ankle deep tendon reflexes grade /IV, left extensor cutaneous plantar response, and spastic gait.[scielo.br]

  • Autosomal Recessive Spastic Paraplegia Type 48

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

  • 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[rarediseases.org] Hereditary spastic paraplegia ( HSP ) is a group of inherited diseases whose main feature is a progressive gait disorder.[en.wikipedia.org] SPG4 is characterized by insidiously progressive bilateral lower-limb gait spasticity.[centogene.com]

  • Wilson Disease

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

  • Infantile Dystonia - Parkinsonism

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

  • Paraplegia

    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[rarediseases.org] ., coarse features, bulbous nose and hypomimia); (c) developmental delay and intellectual disability; (d) early-onset spastic weakness of the lower limbs; and (e) cerebellar[ncbi.nlm.nih.gov] Patients with degenerative neurological diseases such as cerebellar ataxia, spastic paraplegia, and Parkinson's disease often display progressive gait function decline that[ncbi.nlm.nih.gov]

  • Spastic Paraplegia

    Initial symptoms that make be experienced are mild difficulties in walking style (causing what is called a spastic gait) and mild leg stiffness.[mda.org.nz] ., coarse features, bulbous nose and hypomimia); (c) developmental delay and intellectual disability; (d) early-onset spastic weakness of the lower limbs; and (e) cerebellar[ncbi.nlm.nih.gov] He described “a pure spastic movement disorder of the legs” in 2 brothers who developed a spastic gait at the ages of 37 and 56 years.[medlink.com]

  • Autosomal Dominant Spastic Paraplegia Type 31

    ; Spastic gait ; Spastic paraplegia ; Talipes equinovarus[genedx.com] Walking difficulties with imbalance, speech problems, and slowness, progressively stiff and he complained of leg weakness and falls, brisk reflexes, ankle clonus Facial hypomimia[movementdisorders.org] 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[1pdf.net]

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