Literature DB >> 29930972

The Spectrum of Movement Disorders in Childhood-Onset Lysosomal Storage Diseases.

Darius Ebrahimi-Fakhari1,2, Clara Hildebrandt2,3, Peter E Davis1, Lance H Rodan3, Irina Anselm1, Olaf Bodamer3,4.   

Abstract

BACKGROUND: Movement disorders are a significant clinical problem in lysosomal storage diseases (LSD) and account for substantial morbidity. The spectrum of movement disorders in childhood-onset LSD, however, remains poorly defined.
OBJECTIVES: To define the spectrum of movement disorders in a well-characterized cohort of children with LSD.
METHODS: A retrospective chart review at a single tertiary care center (Boston Children's Hospital, Boston, MA, USA). Patients up to the age of 18 years with a clinical, genetic and/or biochemical diagnosis of an LSD and at least one predefined movement disorder (parkinsonism, dystonia, ataxia, tremor, chorea, myoclonus, ballism, restless leg syndrome) were included.
RESULTS: 96 patients were identified and 76 patients had a sufficiently document biochemical and/or genetic diagnosis. Of these, 18 patients met inclusion criteria (mean age: 10.3±5.8 (SD) years, range: 3-18 years; 72% male). The most common LSD associated with a movement disorder was Niemann-Pick disease type C (NPC), followed by several types of neuronal ceroid lipofuscinosis (NCL) and different mucopolysaccharidoses. The most common movement disorder was ataxia followed by rest tremor, dystonia and myoclonus. The other predefined movement disorders were rare. The majority of patients presented with more than one movement disorder. The movement disorder was slowly progressive in all patients. Brain MRI changes included diffuse cerebral volume loss, white matter abnormalities with thinning of the corpus callosum, and cerebellar atrophy.
CONCLUSIONS: Movement disorders develop in a significant number of LSD patients. Ataxia, often in patients with NPC and NCL, is the most common phenotype but significant heterogeneity exists within and between different LSD.

Entities:  

Keywords:  Niemann-Pick disease type C; ataxia; lysosomal storage diseases; neurogenetics; neuronal ceroid lipofuscinosis

Year:  2017        PMID: 29930972      PMCID: PMC6005694          DOI: 10.1002/mdc3.12573

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN: 2330-1619


  19 in total

1.  Heterogeneity and frequency of movement disorders in juvenile and adult-onset Niemann-Pick C disease.

Authors:  Mathieu Anheim; Ouhaïd Lagha-Boukbiza; Marie-Céline Fleury-Lesaunier; Maria-Paola Valenti-Hirsch; Edouard Hirsch; Hélène Gervais-Bernard; Emmanuel Broussolle; Stéphane Thobois; Marie T Vanier; Philippe Latour; Christine Tranchant
Journal:  J Neurol       Date:  2013-11-01       Impact factor: 4.849

2.  Movement disorders associated with chronic GM2 gangliosidosis. Case report and review of the literature.

Authors:  C E Oates; E P Bosch; M N Hart
Journal:  Eur Neurol       Date:  1986       Impact factor: 1.710

3.  Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations.

Authors:  Laura Canafoglia; Isabella Gilioli; Federica Invernizzi; Vito Sofia; Valeria Fugnanesi; Michela Morbin; Luisa Chiapparini; Tiziana Granata; Simona Binelli; Vidmer Scaioli; Barbara Garavaglia; Nardo Nardocci; Samuel F Berkovic; Silvana Franceschetti
Journal:  Neurology       Date:  2015-06-26       Impact factor: 9.910

Review 4.  Dystonia and parkinsonism in GM1 type 3 gangliosidosis.

Authors:  Emmanuel Roze; Eduard Paschke; Nathalie Lopez; Thomas Eck; Kunihiro Yoshida; Annie Maurel-Ollivier; Diane Doummar; Catherine Caillaud; Damien Galanaud; Thierry Billette de Villemeur; Marie Vidailhet; Anne Roubergue
Journal:  Mov Disord       Date:  2005-10       Impact factor: 10.338

Review 5.  Treatable inherited rare movement disorders.

Authors:  H A Jinnah; Alberto Albanese; Kailash P Bhatia; Francisco Cardoso; Gustavo Da Prat; Tom J de Koning; Alberto J Espay; Victor Fung; Pedro J Garcia-Ruiz; Oscar Gershanik; Joseph Jankovic; Ryuji Kaji; Katya Kotschet; Connie Marras; Janis M Miyasaki; Francesca Morgante; Alexander Munchau; Pramod Kumar Pal; Maria C Rodriguez Oroz; Mayela Rodríguez-Violante; Ludger Schöls; Maria Stamelou; Marina Tijssen; Claudia Uribe Roca; Andres de la Cerda; Emilia M Gatto
Journal:  Mov Disord       Date:  2017-09-01       Impact factor: 10.338

Review 6.  Clinical features of adult GM1 gangliosidosis: report of three Indian patients and review of 40 cases.

Authors:  Uday Muthane; Yasha Chickabasaviah; Chris Kaneski; Susurla K Shankar; Gayathri Narayanappa; Rita Christopher; Srikanth Subbamma Govindappa
Journal:  Mov Disord       Date:  2004-11       Impact factor: 10.338

7.  Juvenile progressive dystonia: a new phenotype of GM2 gangliosidosis.

Authors:  D Meek; L S Wolfe; E Andermann; F Andermann
Journal:  Ann Neurol       Date:  1984-04       Impact factor: 10.422

8.  Progressive dystonia symptomatic of juvenile GM2 gangliosidosis.

Authors:  N Nardocci; B Bertagnolio; V Rumi; L Angelini
Journal:  Mov Disord       Date:  1992       Impact factor: 10.338

Review 9.  Lysosomal storage diseases--the horizon expands.

Authors:  Rose-Mary Naaman Boustany
Journal:  Nat Rev Neurol       Date:  2013-08-13       Impact factor: 42.937

Review 10.  The lysosomal storage disease continuum with ageing-related neurodegenerative disease.

Authors:  Emyr Lloyd-Evans; Luke J Haslett
Journal:  Ageing Res Rev       Date:  2016-08-08       Impact factor: 10.895

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  6 in total

Review 1.  Skin Conditions and Movement Disorders: Hiding in Plain Sight.

Authors:  Kristina Kulcsarova; Janette Baloghova; Jan Necpal; Matej Skorvanek
Journal:  Mov Disord Clin Pract       Date:  2022-03-24

2.  Neurodegeneration with Progressive Dystonia: Juvenile-Onset Tay-Sachs Disease.

Authors:  Jasmine Kaur; Singanamalla Bhanudeep; Ramprabhu G Suresh; Arushi G Saini; Vikas Bhatia
Journal:  Ann Indian Acad Neurol       Date:  2022-05-17       Impact factor: 1.714

Review 3.  Parkinsonisms and Glucocerebrosidase Deficiency: A Comprehensive Review for Molecular and Cellular Mechanism of Glucocerebrosidase Deficiency.

Authors:  Emilia M Gatto; Gustavo Da Prat; Jose Luis Etcheverry; Guillermo Drelichman; Martin Cesarini
Journal:  Brain Sci       Date:  2019-02-01

Review 4.  KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders.

Authors:  Xinchen Teng; Abdel Aouacheria; Loïc Lionnard; Kyle A Metz; Lucian Soane; Atsushi Kamiya; J Marie Hardwick
Journal:  CNS Neurosci Ther       Date:  2019-07       Impact factor: 5.243

Review 5.  A Proposed Diagnostic Algorithm for Inborn Errors of Metabolism Presenting With Movements Disorders.

Authors:  Juan Darío Ortigoza-Escobar
Journal:  Front Neurol       Date:  2020-11-13       Impact factor: 4.003

6.  Spectrum of Movement Disorders in Niemann-Pick Disease Type C.

Authors:  Rashmi Devaraj; Rohan R Mahale; D M Sindhu; Albert Stezin; Nitish Kamble; Vikram V Holla; M Netravathi; Ravi Yadav; Pramod Kumar Pal
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2022-09-08
  6 in total

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