75 Possible Causes for Hypomimia, Spastic Gait

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  • Autosomal Recessive Spastic Paraplegia Type 49

    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] Medications may help to reduce muscle spasticity and improve gait. The drug, baclofen, is often used to treat spasticity.[cigna.com]

  • Pallidopyramidal Syndrome

    […] fibers 20% Gait disturbance 20% Increased variability in muscle fiber diameter 20% Peripheral neuropathy 20% Impaired distal proprioception 20% Microcephaly 20% Muscle fiber[mendelian.co] Pill-rolling tremor, hypomimia, hypophonia, stooping posture, striatal toes and equinovarous deformity may be noted.[neurologyindia.com] He walked at 1 year, and developed gait impairment at age 6 years. Gait progressively declined, and cognitive impairment was noted in adolescence.[dokumen.tips]

  • 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]

  • Parkinsonian Disorder

    Typically, muscles are of normal strength if given time to develop power. There is no alteration in tendon reflexes or plantar responses.[patient.info] In addition to a general slowness of movement, the bradykinesia of Parkinson’s disease is typically demonstrated by a reduced or mask-like expression of the face (hypomimia[apdaparkinson.org] Delayed postural reflexes refers to a delay in the normal righting responses that permit stance and gait.[dartmouth.edu]

  • Juvenile Paralysis Agitans of Hunt

    Unilateral Extensor Spasticity A spastic gait is common in upper motor neuron diseases that have a spastic paralysis of the extensor muscles.[chiro.org] Hypomimia- “masked facies”,expressionless face, blinking Speech abnormalities- Hypophonia: soft voice Aprosody of speech: monotonous and lack of inflection Tachyphemia: do[slideplayer.com] The facial expression is markedly different from the hypomimia and masking of PD.[neupsykey.com]

  • Parkinson-Dementia Syndrome

    As the disease progresses, people experience increasing cognitive deficits, spasticity, muscle atrophy, and weakness.[secure.ssa.gov] […] strengthening; flexibility, as well as for gait training; Occupational therapy helps to maintain skills and promote function and independence; and, The primary bulbar muscles[secure.ssa.gov] […] inhibitors for the treatment of neuropsychiatric symptoms; Levodopa-carbidopa combinations to treat movement disorders; Physical therapy for cardiovascular and skeletal muscle[secure.ssa.gov]

  • Parkinson's Disease

    Other clinical features include secondary motor symptoms (eg, hypomimia, dysarthria, dysphagia, sialorrhoea, micrographia, shuffling gait, festination, freezing, dystonia,[jnnp.bmj.com] […] bradykinesia include loss of spontaneous movements and gesturing, drooling because of impaired swallowing, 25 monotonic and hypophonic dysarthria, loss of facial expression (hypomimia[jnnp.bmj.com]

  • Parkinson's Disease Type 3
  • Autosomal Recessive Spastic Paraplegia Type 48

    Gait was both spastic and parkinsonian (video 2).[ng.neurology.org] If symptoms begin during the teenage years or later, then spastic gait disturbance usually progresses over many years.[ipfs.io] Hereditary spastic paraplegia ( HSP ) is a group of inherited diseases whose main feature is a progressive gait disorder.[en.wikipedia.org]

  • Neuroferritinopathy

    It is inherited in an autosomal dominant fashion. 0002067 Dysphonia Inability to produce voice sounds 0001618 Dystonia 0001332 Gait disturbance Abnormal gait Abnormal walk[rarediseases.info.nih.gov] While 35% developed facial hypomimia and bradykinesia not directly related to their dystonia; only one individual developed a pure rest tremor, and another had tremor present[academic.oup.com] Spasticity and muscle rigidity usually begin in the legs and later develop in the arms.[nbiaalliance.org]

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