Literature DB >> 30363497

Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings.

Kristina K Grim1, Gregory D Phillips1, David R Renner1.   

Abstract

Late-onset Tay-Sachs disease (LOTS) is a rare autosomal-recessive genetic disorder caused by insufficient activity of the lysosomal enzyme, beta-hexosaminidase A, resulting in intracellular accumulation of gangliosides in the central nervous system. Clinical manifestations can include unsteadiness in gait, muscle weakness, cognitive dysfunction, psychiatric disturbance, and dysarthric speech. The variable presentation of these symptoms, combined with the late onset of the disease, often results in misdiagnosis. We present video of 3 sibling cases of LOTS in which a dysarthric stutter was the sole presenting symptom in order to better characterize the phenotype of this disease.

Entities:  

Keywords:  GM2 gangliosidosis; Tay‐Sachs disease; dysarthria; hexosaminidase A; stutter

Year:  2015        PMID: 30363497      PMCID: PMC6178690          DOI: 10.1002/mdc3.12194

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


  8 in total

1.  Ataxia and weakness in a young woman.

Authors:  Shin Chien Beh; Sharon Nations; Juan M Pascual; Steven Vernino
Journal:  Arch Neurol       Date:  2012-07

2.  Achalasia in a patient with adult-onset Tay-Sachs disease.

Authors:  Jeffrey W Nathanson; Charles S Winans
Journal:  Dig Dis Sci       Date:  2006-01       Impact factor: 3.199

3.  Late-onset Tay-Sachs disease presenting as a childhood stutter.

Authors:  B E Shapiro; M R Natowicz
Journal:  J Neurol Neurosurg Psychiatry       Date:  2009-01       Impact factor: 10.154

4.  Late-onset hexosaminidase A deficiency mimicking primary lateral sclerosis.

Authors:  Clecio Godeiro-Junior; Andre C Felicio; Vinicius Benites; Marco Antonio Chieia; Acary S B Oliveira
Journal:  Arq Neuropsiquiatr       Date:  2009-03       Impact factor: 1.420

5.  Late-onset Tay-Sachs disease: phenotypic characterization and genotypic correlations in 21 affected patients.

Authors:  Orit Neudorfer; Gregory M Pastores; Bai J Zeng; John Gianutsos; Charles M Zaroff; Edwin H Kolodny
Journal:  Genet Med       Date:  2005-02       Impact factor: 8.822

Review 6.  The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported.

Authors:  Gustavo H B Maegawa; Tracy Stockley; Michael Tropak; Brenda Banwell; Susan Blaser; Fernando Kok; Roberto Giugliani; Don Mahuran; Joe T R Clarke
Journal:  Pediatrics       Date:  2006-10-02       Impact factor: 7.124

7.  Late onset GM2 gangliosidosis mimicking spinal muscular atrophy.

Authors:  Z Jamrozik; A Lugowska; M Gołębiowski; L Królicki; J Mączewska; M Kuźma-Kozakiewicz
Journal:  Gene       Date:  2013-06-29       Impact factor: 3.688

8.  Progressive cerebellar ataxia, proximal neurogenic weakness and ocular motor disturbances: hexosaminidase A deficiency with late clinical onset in four siblings.

Authors:  E Hund; A Grau; W Fogel; M Forsting; M Cantz; B Kustermann-Kuhn; K Harzer; R Navon; H H Goebel; H M Meinck
Journal:  J Neurol Sci       Date:  1997-01       Impact factor: 3.181

  8 in total
  5 in total

1.  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

2.  Quantitative oculomotor and nonmotor assessments in late-onset GM2 gangliosidosis.

Authors:  Christopher D Stephen; David Balkwill; Peter James; Elizabeth Haxton; Kenneth Sassower; Jeremy D Schmahmann; Florian Eichler; Richard Lewis
Journal:  Neurology       Date:  2020-01-21       Impact factor: 9.910

3.  The GM2 gangliosidoses: Unlocking the mysteries of pathogenesis and treatment.

Authors:  Camilo Toro; Mosufa Zainab; Cynthia J Tifft
Journal:  Neurosci Lett       Date:  2021-08-25       Impact factor: 3.046

4.  Oromandibular Dystonia - A Systematic Review.

Authors:  Udit Saraf; Mitesh Chandarana; K P Divya; Syam Krishnan
Journal:  Ann Indian Acad Neurol       Date:  2021-10-22       Impact factor: 1.383

5.  Magnetic resonance imaging and spectroscopy in late-onset GM2-gangliosidosis.

Authors:  Olivia E Rowe; D Rangaprakash; Akila Weerasekera; Neha Godbole; Elizabeth Haxton; Peter F James; Christopher D Stephen; Robert L Barry; Florian S Eichler; Eva-Maria Ratai
Journal:  Mol Genet Metab       Date:  2021-06-24       Impact factor: 4.204

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.