Literature DB >> 27928380

Facial Dystonia with Facial Grimacing and Vertical Gaze Palsy with "Round the Houses" Sign in a 29-Year-Old Woman.

J Crespi1, G Bråthen1, P Quist-Paulsen2, J Pagonabarraga3, C Roig-Arnall3.   

Abstract

A 29-year-old woman developed progressive dysarthria and coordination problems from the age of 15. Examination showed dysarthria, facial dystonia, bibrachial dystonia, hyperreflexia, ataxia, and emotional incontinence. Downward supranuclear gaze palsy was prominent with a "Round the Houses" sign. Magnetic resonance imaging of the brain and medulla, electroneurography, and cerebrospinal fluid were normal. A computed tomography scan showed hepatosplenomegaly. This combination of progressive neurological symptoms together with hepatosplenomegaly was suggestive of inborn error of metabolism. A bone marrow biopsy showed an increased number of macrophages with foamy content, highly suggestive of lysosomal disease. Plasmatic chitotriosidase activity and CCL18 were increased. Genetic testing showed heterozygosis for the variation c.1070C→T (p.Ser357Leu) and c.1843→T (Arg615Cys), confirming the diagnosis of Niemann-Pick type C (NPC). The "Round the Houses" sign has only been described in patients with progressive supranuclear palsy (PSP). This sign is described as an inability to produce pure vertical saccades along the midline and instead moving the eyes in a lateral arc to accomplish the movement. The observation of this sign in a patient with NPC indicates that this bedside finding is not specific for PSP, but a sign of medial longitudinal fasciculus dysfunction. The presence of facial dystonia with facial grimacing together with supranuclear gaze palsy is highly characteristic and useful for the diagnosis of NPC. NPC is an important underdiagnosed condition, given the availability of treatment and a mean diagnostic delay of 6 years.

Entities:  

Keywords:  Inborn error of metabolism; Niemann Pick type C; lysosomal disease; miglustat; vertical gaze palsy; “Round the Houses” sign

Year:  2016        PMID: 27928380      PMCID: PMC5123166          DOI: 10.3109/01658107.2015.1105824

Source DB:  PubMed          Journal:  Neuroophthalmology        ISSN: 0165-8107


  8 in total

1.  CCL18 as an alternative marker in Gaucher and Niemann-Pick disease with chitotriosidase deficiency.

Authors:  Kai-Ling Chang; Wuh-Liang Hwu; Hui-Ying Yeh; Ni-Chung Lee; Yin-Hsiu Chien
Journal:  Blood Cells Mol Dis       Date:  2009-10-09       Impact factor: 3.039

2.  Development of a suspicion index to aid diagnosis of Niemann-Pick disease type C.

Authors:  F A Wijburg; F Sedel; M Pineda; C J Hendriksz; M Fahey; M Walterfang; M C Patterson; J E Wraith; S A Kolb
Journal:  Neurology       Date:  2012-04-18       Impact factor: 9.910

3.  Niemann-Pick type C disease: accelerated neurofibrillary tangle formation and amyloid beta deposition associated with apolipoprotein E epsilon 4 homozygosity.

Authors:  Yuko Saito; Kinuko Suzuki; Eiji Nanba; Toshiyuki Yamamoto; Kousaku Ohno; Shigeo Murayama
Journal:  Ann Neurol       Date:  2002-09       Impact factor: 10.422

4.  Recommendations on the diagnosis and management of Niemann-Pick disease type C.

Authors:  James E Wraith; Matthias R Baumgartner; Bruno Bembi; Athanasios Covanis; Thierry Levade; Eugen Mengel; Mercè Pineda; Frédéric Sedel; Meral Topçu; Marie T Vanier; Hakan Widner; Frits A Wijburg; Marc C Patterson
Journal:  Mol Genet Metab       Date:  2009-06-14       Impact factor: 4.797

5.  Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study.

Authors:  Marc C Patterson; Darleen Vecchio; Helena Prady; Larry Abel; James E Wraith
Journal:  Lancet Neurol       Date:  2007-09       Impact factor: 44.182

6.  Dynamic properties of horizontal and vertical eye movements in parkinsonian syndromes.

Authors:  K G Rottach; D E Riley; A O DiScenna; A Z Zivotofsky; R J Leigh
Journal:  Ann Neurol       Date:  1996-03       Impact factor: 10.422

7.  Identification of 58 novel mutations in Niemann-Pick disease type C: correlation with biochemical phenotype and importance of PTC1-like domains in NPC1.

Authors:  Walter D Park; John F O'Brien; Patrick A Lundquist; Daniel L Kraft; Cate Walsh Vockley; Pamela S Karnes; Marc C Patterson; Karen Snow
Journal:  Hum Mutat       Date:  2003-10       Impact factor: 4.878

8.  Saccades in adult Niemann-Pick disease type C reflect frontal, brainstem, and biochemical deficits.

Authors:  L A Abel; M Walterfang; M Fietz; E A Bowman; D Velakoulis
Journal:  Neurology       Date:  2009-03-24       Impact factor: 9.910

  8 in total
  4 in total

1.  The Area under the Main Sequence as an Alternative Method to Measure Saccadic Dynamics.

Authors:  Claudio Busettini; Jennifer Braswell Christy
Journal:  Optom Vis Sci       Date:  2018-11       Impact factor: 1.973

2.  Patient with Niemann-Pick disease type C: over 20 years' follow-up.

Authors:  Kazuo Abe; Norio Sakai
Journal:  BMJ Case Rep       Date:  2017-08-22

Review 3.  Clinical Approach to Supranuclear Brainstem Saccadic Gaze Palsies.

Authors:  Alexandra Lloyd-Smith Sequeira; John-Ross Rizzo; Janet C Rucker
Journal:  Front Neurol       Date:  2017-08-23       Impact factor: 4.003

Review 4.  How to spot ocular abnormalities in progressive supranuclear palsy? A practical review.

Authors:  Onanong Phokaewvarangkul; Roongroj Bhidayasiri
Journal:  Transl Neurodegener       Date:  2019-07-10       Impact factor: 8.014

  4 in total

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