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Adult-onset Idiopathic Focal Lower Extremity Dystonia: A Rare Task-Specific Dystonia

Authors:

Ritesh A. Ramdhani ,

Movement Disorders Division, Mount Sinai School of Medicine, New York, New York, US
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Steven J. Frucht

Movement Disorders Division, Mount Sinai School of Medicine, New York, New York, US
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Abstract

Background: Adult-onset focal lower extremity (LE) dystonia is rare, but there have recently been a number of case series that have reported an idiopathic variant triggered during ambulation.

Methods: We describe nine patients with idiopathic, focal task-specific LE dystonia. We conducted a comparative analysis that included our cohort and several recently published case series to further characterize the disorder.

Results: A total of 48 patients (37 female, 11 male) were compared. The average age of onset was 48 years; 36 patients had distal extremity involvement (75%), 5 proximal (10%), and 7 both proximal and distal (15%). Among 33 patients in which the dystonic side was known, 20 were affected on the left (61%). Inversion of the foot with flexion of one or more toes was the most prevalent pattern in those with distal extremity involvement.

Discussion: This is a novel task-specific dystonia triggered during ambulation that is often misdiagnosed as an orthopedic or psychogenic issue.

How to Cite: Ramdhani RA, Frucht SJ. Adult-onset Idiopathic Focal Lower Extremity Dystonia: A Rare Task-Specific Dystonia. Tremor and Other Hyperkinetic Movements. 2013;3:tre-03-142-2990-1. DOI: http://doi.org/10.5334/tohm.135
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  Published on 22 Jan 2013
 Accepted on 26 Nov 2012            Submitted on 23 Oct 2012

Introduction

Focal task-specific dystonias (FTSDs) usually affect the upper limbs or craniocervical regions (e.g., writer's cramp, musician's hand dystonia, or embouchure dystonia). Lower extremity (LE) dystonia is thought to be rare in adults and more common in children. When it does occur in adults, it tends to be non-task specific and is often associated with parkinsonism, trauma, stroke, or psychogenic behavior. Over the last several years, numerous case reports13 and series47 have highlighted an unusual task-specific dystonia with ambulatory triggers. Here, we describe nine patients with idiopathic, focal task-specific LE dystonia and compare them to several recently published case series to call attention to the condition.

Case series

Among the patients we encountered (Table 1), the average age was 49.3 years with females outnumbering males (2:1). The average age of symptom onset was 45.6 years with an average time to diagnosis of 3.7 years. Many patients had extensive workups, including normal imaging studies, prior to being seen in our center. None had received dopamine receptor blocking agents or had experienced prior central nervous system insult.

Table 1.

Mount Sinai Case Series

Patient # Age/Sex Onset Age Duration (yrs) Limb Precipitant Movement Task Phenomenology Present at Rest Other Limbs Affected FH Medications Response
1 31/M 26 5 R Walking down steps Plantarflexes foot and flexes hip when walking down steps. Absent while walking up steps or backward. No None PD Sinemet None
2 24/F 20 4 L Marathon running Inversion and plantarflexion of the foot while walking that becomes more prominent with running. Does not occur when walking backward. No None None Sinemet None
3 33/F 31 2 R Marathon running Sustained inversion while walking, which normalizes while walking backward. Improves with side stepping in either direction as well as walking forward while imagining walking backward. No None None Sinemet Artane Baclofen BTX to calf Valium None None None None Yes
4 60/F 58 2 L Distance walking Hip flexion with slight side to side lurch while walking. Improves with imagined walking backward while walking forward. No None Mother & Father - PD Klonopin Artane None None
5 61/M 58 3 R Walking Eversion of foot while walking on cobblestone terrain or walking down steps. Disappears while walking on flat surfaces, running, or climbing stairs. No None Mother - similar movements Sinemet None
6 27/F 22 5 L Distance running Inversion and sustained plantarflexion of the foot while walking. Movements disappeared while walking backward ,as well as imagined walking backward while walking forward. No abnormal movements when climbing stairs or during side stepping. No None None Artane None
7 80/M 78 2 R Walking Eversion of foot while walking that disappears while walking backward or sideways and climbing stairs. No Yes - R Wrist 'Yips' None Sinemet None
8 53/F 49 4 L Walking Curling of toes and inversion of foot while walking, which is also produced with foot tapping. No None None BTX Klonopin Gabapentin Yes Yes Yes
9 75/F 69 6 R Walking Hyperextension and abduction of leg. More prominent with speed walking. No None None Sinemet Ropinerole None None
Mean 49.3 45.6 3.7

Lower limb dystonia (five right, four left) was triggered by ambulation in all nine patients and was not present at rest. Six patients had distal extremity involvement, two patients demonstrated proximal involvement (i.e., hip flexion, hyperextension, and abduction), and one patient exhibited both proximal and distal extremity involvement (i.e., hip flexion with foot plantar flexion). Foot inversion was the most common pattern (4/9 patients), with two patients having concomitant plantar flexion. One patient (Patient 9) had involvement of the toes along with foot inversion. Walking backward or simply imagining walking backward while walking forward often improved symptoms. One patient (Patient 7) had coincident R wrist ‘yips’ or golfer’s cramp. Treatment with L-dopa (0/5 patients) was ineffective, but one of two patients treated with botulinum toxin injections improved.

Adding our cases to those published previously yielded a total of 48 patients (37 female, 11 male) diagnosed with idiopathic FTSD of the LE. Comparative analysis of these patients (Table 2) revealed that 36 had distal extremity involvement (75%), 5 demonstrated proximal (10%), and 7 both proximal and distal (15%). The average age of symptom onset was 48 years old, and family history of dystonia was rare. Among 33 patients in whom the side of the dystonia was known, 20 were affected on the left (61%). Routine ambulatory tasks (e.g., standing, walking, ascending or descending stairs) were triggers of the dystonic limb posture, and only six patients (13%) had dystonia at rest. Concomitant upper extremity dystonia was observed in three patients, and one had cervical dystonia.

Table 2.

Focal Task-Specific Lower Extremity Dystonia Comparative Analysis

Case Series Patients
Sex
Idiopathic Cases
Average Age of Onset
FH of Movement Disorders
Limb Affected (Idiopathic)
Other Body Parts
Present at Rest
No. M F M F (yrs) R L Both
Singer and Papapetropoulus4 4 1 3 1 3 59.5 x 0 4 0 0/4 2
Schneider et al.5 17 6 11 5 11 48.2 PD - 1 LD -2 Hand Tremor - 1 7 8 1 2/15 (arm, cervical dystonia) NR
Wu and Jankovic6 5 2 3 2 3 37.4 0 1 4 0 0/5 0
McKeon et al.7 36 5 31 0 14 51.1 NR NR NR NR 0/14 4
MSMC 9 3 6 3 6 45.7 PD - 2 LD - 1 5 4 0 1/9(yips) 0
Total 71</emph> 17</emph> 54</emph> 11</emph> 37 48.38 13 20 1 6

Abbreviations: (FH, Family History; PF, Plantarflexion; DF, Dorsiflexion; (+), presence; (−), absence; NR, not reported; PD, Parkinson1s Disease; LD, Limb dystonia; BTX, Botulinum Toxin; MSMC, Mount Sinai Medical Centre).

Analysis of the 43 patients with distal extremity involvement revealed that 29 (67%) had a predilection for foot inversion, and 14 of those 29 patients (48%) exhibited concomitant plantar flexion. Pure ankle eversion (three patients), foot plantar flexion (four patients) and foot dorsiflexion (two patients) were less common. Toe movements described as either dorsi- or plantar flexion of one or more toes were observed in 21 of 43 patients (49%), with 19 of those 21 patients (90%) having associated dystonic posturing of the foot.

Compared to other types of FTSD, LE dystonia manifests at a later age and predominantly affects females (F): Musician’s hand (36 yrs/F20%),8 Writer’s Cramp (38 yrs/F33%),8 Embouchure (36 yrs/F28%),8 Cranial (46 yrs/F43%),8 LE (48 yrs/F77%). These FTSDs share features such as lack of spread to other limbs and absence of trauma as an underlying factor.

Discussion

All nine patients in our case series had unremarkable medical histories; none exhibited signs of psychogenic behavior,9, 10 such as fixed dystonia, inconsistency, incongruency, or weakness upon examination. There were no histories of mood disorders or pending litigation. Parkinsonism was not present at onset and had not developed during 4 years of follow up. This is similar to what was observed in the other four cases series. Because DYT-1 dystonia11 usually begins in the LE, especially in those younger than 26 years, Patients 1 and 6 were tested and found to be negative, whereas Patients 2 and 3 were referred for testing but did not do so.

LE movements had several factors in common in all 48 patients of the comparative analysis. First, various ambulatory tasks (e.g., walking, walking down steps, running) were specific triggers for the dystonic posturing, which was rarely present at rest and failed to spread to other limbs. Second, exteroceptive sensory gestes, such as walking backward and side stepping, as well as the interoceptive sensory geste12 of imagining an external sensory trick (e.g., walking backward) while simultaneously walking forward led to improvement in 6 of 9 patients in our series, as well as many others in the cumulative series (2/4 patients in Singer and Papapetropoulus,4 3/5 patients in Wu and Jankovi,6 and 6/14 patients in McKeon et al.7).

The pathophysiology of this dystonia is unclear, and like most other dystonias, it is the result by both genetic and environmental factors.13 In 15 patients, the initial presentation occurred during prolonged exercise, long distance running, or long distance walking, suggesting a transformation from intense exertion-induced dystonia to one that is easily triggered by routine ambulation. Although it can also be argued that this is a phenomenon of paroxysmal kinesogenic or exertion-induced dyskinesias, the constancy and immediate triggering of the dystonia suggests otherwise. The later age of onset, as well as the considerable number of patients who developed dystonia in the setting of prolonged exertion, further insinuates that repetitive use of a limb14 may peripherally stimulate a change in cortical and/or striatal plasticity, perhaps triggering the dystonic network. The loss of specificity over time may also be a manifestation of surround inhibition failure.13

It is important that physicians recognize this entity as a task-specific dystonia triggered by various modes of ambulation. Many of our patients were misdiagnosed as having orthopedic problems or manifesting psychogenic behavior. The later age of onset, female predominance, and specific foot movement patterns of plantar flexion, inversion, and toe(s) involvement with sensory geste reduction offer clues to its diagnosis. Botulinum toxin injections seem to be most effective treatment across all case series.

Video. 

Patient 1 has Right Hip Flexion while Walking Down Steps.

Video. 

Patient 2 Exhibits Right Foot Inversion while Walking Forward.

Video. 

Patient 3 has Inversion and Sustained Plantar Flexion of the Left Foot while Walking Forward.

Video. 

Patient 4 has Inversion of the Left Foot with Toe Curling while Walking Forward.

Notes

1 Funding: None. 

2 Financial Disclosures: None. 

3 Conflict of Interest: The authors report no conflicts of interest. 

References

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