Abstract

BackgroundPure akinesia with gait freezing is a rare syndrome with few autopsied cases. Severe freezing of gait occurs in the absence of bradykinesia and rigidity. Most autopsies have revealed progressive supranuclear palsy. We report the clinical and postmortem findings of two patients with pure akinesia with gait freezing, provide video recordings of these patients, and review the literature describing similar cases. We also discuss bradykinesia, hypokinesia and akinesia in the context of this clinical syndrome.Case presentationTwo patients with the syndrome of pure akinesia with gait freezing were examined by the same movement disorder specialist at least annually for 9 and 18 years. Both patients initially exhibited freezing, tachyphemia, micrographia and festination without bradykinesia and rigidity. Both autopsies revealed characteristic tau pathology of progressive supranuclear palsy, with nearly total neuronal loss and gliosis in the subthalamus and severe neuronal loss and gliosis in the globus pallidus and substantia nigra. Previously published postmortem studies revealed that most patients with this syndrome had progressive supranuclear palsy or pallidonigroluysian atrophy.ConclusionsPallidonigroluysian degeneration produces freezing and festination in the absence of generalized slowing (bradykinesia). Freezing and festination are commonly regarded as features of akinesia. Akinesia literally means absence of movement, and akinesia is commonly viewed as an extreme of bradykinesia. The pure akinesia with gait freezing phenotype illustrates that bradykinesia and akinesia should be viewed as separate phenomena.

Highlights

  • Pure akinesia with gait freezing is a rare syndrome with few autopsied cases

  • Akinesia literally means absence of movement, and akinesia is commonly viewed as an extreme of bradykinesia

  • The pure akinesia with gait freezing phenotype illustrates that bradykinesia and akinesia should be viewed as separate phenomena

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Summary

Conclusions

The syndrome of PAGF is most commonly caused by PSP. The PSP-PAGF phenotype illustrates that akinesia is not an extreme of bradykinesia because patients with PSP-PAGF initially are not slow. This is patient 1 at age 69, three years after the onset of symptoms. He had no rescue response to the pull test He exhibited festination and decrement in volume/amplitude of his speech and repetitive hand movements, but he had no bradykinesia, rigidity, or tremor. Six years after video 1, patient 1 exhibited generalized bradykinesia and rigidity, increased freezing, upward gaze paresis, slow downward saccades, eyelid paratonia, and severe tachyphemia. Patient 2 at age 71 had a six-year history of tachyphemia, micrographia and freezing gait Her examination revealed tachyphemia, festination and decrement in repetitive hand movements, cautious gait, freezing, absent postural rescue response, and normal tandem gait

Background
Discussion
Progressive supranuclear palsy 1 Lewy body Parkinson disease
Availability of data and materials Not applicable
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