- Letter to the Editor
- Open Access
Upper facial chorea in Huntington disease
© Fekete and Jankovic; licensee BioMed Central Ltd. 2014
- Received: 27 April 2014
- Accepted: 20 June 2014
- Published: 20 November 2014
To provide a systematic description of component movements of upper facial chorea in Huntington disease, consecutive videos of 25 active patients with confirmed diagnosis were scored on eye opening, eye closing, and procerus/corrugator contractions. Of the 25 patients evaluated, 76% exhibited intermittently widened palpebral fissures associated with frontalis contractions. Brief periods of repetitive but irregular blinking were observed in 16%. 8% had brief spasms of the orbital portion of the orbicularis oculi muscles. In addition, brief contractions of procerus and corrugator supercilii muscles were noted in 52%.
- Huntington disease
In his seminal description of the disorder which now bears his name, George Huntington noted that “the eyelids are kept winking, the brows are corrugated, and then elevated, the nose is screwed first to the one side and then to the other, and the mouth is drawn in various directions” [1, 2]. More detailed descriptive information about facial chorea in Huntington disease (HD) is lacking in modern literature. We have systematically studied involuntary movements in the face of patients with documented HD to further characterize upper facial chorea.
Rating scales used for eye closing, eye opening, and procerus/corrugator supercilii contractions
Rare or absent eyeblinks
Normal rate of blinking
Fast rate of eye blinks
Continuous repetitive blinking
Eyes partially closed
Normal eye opening
Moderately increased frequency of eye openings
Markedly enlarged palpebral fissure but without eyebrow elevation or frontalis contractions
Markedly enlarged palpebral fissure with marked eyebrow elevation and frontalis contractions
Demographic and genetic details of patient cohort
Age at diagnosis (years)
Average age (years)
CAG repeat length average*
CAG repeat range*
UHDRS total motor score**
50 ± 16
35 ± 19
In this study of 25 HD patients, upper facial chorea manifested chiefly by brief, irregular widening of palpebral fissures and intermittent, irregular blinking. This phenomenological characterization may be used in the differential diagnosis of facial dyskinesias. Although we acknowledge limitations of this small study, including small sample size and the use of a single rater, we believe that this careful examination of upper face chorea provides useful information about the phenomenology of this movement disorder.
Chorea is characterized by brief, rapid, irregular and random movements that may involve any part of the body. Patients with HD often tend to camouflage the movements by incorporating them into semipurposeful movements (“parakinesia”), which may delay the recognition of chorea and initially hamper the diagnosis. In some cases, facial movements associated with HD may be difficult to differentiate from those observed in patients with other facial dyskinesia such as blepharospasm, tardive dyskinesia, tics, and even hemifacial spasms . Although we did not compare our patients with HD with those of other abnormal movement disorders involving the face, partly because of because of the broad spectrum of phenomenology we believe that we can make some clinical observation that may be helpful in differentiating upper face chorea from other facial dyskinesias. While bilateral orbicularis oculi contractions occur in blepharospasm, the combination of abnormal eye opening and corrugator supercilii contractions in HD should distinguish upper facial movements in these two disorders. Furthermore, the periorbital contractions associated with HD are brief, irregular and random in contrast to more patterned and sustained contractions typically present in patients with blepharospasm. Rare bilateral hemifacial spasm has been reported , but the “other Babinski sign”  manifested by elevation of the eyebrow due to ipsilateral frontalis contraction and simultaneous orbicularis oculi contraction leading to eye closure, typically seen in the setting of hemifacial spams, has not been seen in HD. Instead, frontalis contractions in HD are associated with eye opening (Additional file 1). Upper facial motor tics pose a diagnostic challenge, especially when there are no associated motor or phonic tics, but the presence of premonitory sensation should assist in distinguishing facial tics from chorea . Of note, rare cases of motor as well as vocal tics with premonitory sensation as presenting signs of HD have been reported .Upper facial involvement is rare in tardive dyskinesia, another movement disorder typically involving the face .
In conclusion, the primary aim of study was to draw attention to involvement of upper face in HD and to note that the appropriate recognition of the phenomenology should lead to the correct diagnosis and appropriate treatment .
We thank Cathy Jankovic for videotape editing.
- Lanska DJ: George Huntington and hereditary chorea. J Child Neurol 1995, 10: 46–48. 10.1177/088307389501000112View ArticlePubMedGoogle Scholar
- Huntington G: On chorea. Med Surg Rep Wkly J 1872,26(15):317–321.Google Scholar
- Jankovic J, Kenney C, Grafe S, Goertelmeyer R, Comes G: Relationship between various clinical outcome assessments in patients with blepharospasm. Mov Disord 2009, 24: 407–413. 10.1002/mds.22368View ArticlePubMedGoogle Scholar
- Yaltho TC, Jankovic J: The many faces of hemifacial spasm: Differential diagnosis of unilateral facial spasms. Mov Disord 2011, 26: 1582–1592. 10.1002/mds.23692View ArticlePubMedGoogle Scholar
- Stamey W, Jankovic J: The other Babinski sign in hemifacial spasm. Neurology 2007, 69: 402–403. 10.1212/01.wnl.0000266389.52843.3bView ArticlePubMedGoogle Scholar
- Jankovic J, Ashizawa T: Tourettism associated with Huntington’s disease. Mov Disord 1995, 10: 103–105. 10.1002/mds.870100116View ArticlePubMedGoogle Scholar
- Jankovic J: Drug-induced and other orofacial-cervical dyskinesias. Ann Intern Med 1981, 94: 788–793. 10.7326/0003-4819-94-6-788View ArticlePubMedGoogle Scholar
- Jankovic J: Treatment of hyperkinetic movement disorders. Lancet Neurol 2009, 8: 844–856. 10.1016/S1474-4422(09)70183-8View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.