Literature DB >> 9547461

Neuropsychiatric aspects of the adult variant of Tay-Sachs disease.

G M MacQueen1, P I Rosebush, M F Mazurek.   

Abstract

Tay-Sachs disease (a GM2 gangliosidosis) is an inherited neuronal storage disease that can affect individuals across the age spectrum. Psychosis is reported in 30% to 50% of adult-onset patients, and many are misdiagnosed with schizophrenia. Mood disorders are present in more than 25% and cognitive impairment in more than 20%. Treatment of psychosis with neuroleptics may not have a favorable risk/benefit ratio, but treatment with benzodiazepines or electroconvulsive therapy may be efficacious. Metabolic diseases such as gangliosidosis are probably under-recognized as causes of neuropsychiatric illness. Increased awareness of these disorders will lead to accurate diagnosis, appropriate treatment selection, and genetic counseling.

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Year:  1998        PMID: 9547461     DOI: 10.1176/jnp.10.1.10

Source DB:  PubMed          Journal:  J Neuropsychiatry Clin Neurosci        ISSN: 0895-0172            Impact factor:   2.198


  16 in total

1.  Paranoid delusion as lead symptom in two siblings with late-onset Tay-Sachs disease and a novel mutation in the HEXA gene.

Authors:  Claudia Stendel; Constanze Gallenmüller; Katrin Peters; Friederike Bürger; Gwendolyn Gramer; Saskia Biskup; Thomas Klopstock
Journal:  J Neurol       Date:  2015-04-11       Impact factor: 4.849

Review 2.  Psychiatric and Cognitive Symptoms Associated with Niemann-Pick Type C Disease: Neurobiology and Management.

Authors:  Thomas Rego; Sarah Farrand; Anita M Y Goh; Dhamidhu Eratne; Wendy Kelso; Simone Mangelsdorf; Dennis Velakoulis; Mark Walterfang
Journal:  CNS Drugs       Date:  2019-02       Impact factor: 5.749

3.  Amyotrophy, cerebellar impairment and psychiatric disease are the main symptoms in a cohort of 14 Czech patients with the late-onset form of Tay-Sachs disease.

Authors:  Helena Jahnová; Helena Poupětová; Jitka Jirečková; Hana Vlášková; Eva Košťálová; Radim Mazanec; Alena Zumrová; Petr Mečíř; Zuzana Mušová; Martin Magner
Journal:  J Neurol       Date:  2019-05-10       Impact factor: 4.849

Review 4.  Frontotemporal dementia: a bridge between dementia and neuromuscular disease.

Authors:  Adeline S L Ng; Rosa Rademakers; Bruce L Miller
Journal:  Ann N Y Acad Sci       Date:  2014-12-30       Impact factor: 5.691

Review 5.  Genetic counselling for schizophrenia in the era of molecular genetics.

Authors:  K A Hodgkinson; J Murphy; S O'Neill; L Brzustowicz; A S Bassett
Journal:  Can J Psychiatry       Date:  2001-03       Impact factor: 4.356

Review 6.  Therapeutic Strategies For Tay-Sachs Disease.

Authors:  Jaqueline A Picache; Wei Zheng; Catherine Z Chen
Journal:  Front Pharmacol       Date:  2022-07-05       Impact factor: 5.988

Review 7.  The neuropsychiatry of inborn errors of metabolism.

Authors:  Mark Walterfang; Olivier Bonnot; Ramon Mocellin; Dennis Velakoulis
Journal:  J Inherit Metab Dis       Date:  2013-05-23       Impact factor: 4.982

8.  Early deficits in motor coordination and cognitive dysfunction in a mouse model of the neurodegenerative lysosomal storage disorder, Sandhoff disease.

Authors:  Maria Gulinello; Fengying Chen; Kostantin Dobrenis
Journal:  Behav Brain Res       Date:  2008-06-20       Impact factor: 3.332

Review 9.  Nosology and Phenomenology of Psychosis in Movement Disorders.

Authors:  Malco Rossi; Nicole Farcy; Sergio E Starkstein; Marcelo Merello
Journal:  Mov Disord Clin Pract       Date:  2020-01-07

10.  Late-Onset Tay-Sachs Disease in an Irish Family.

Authors:  Stela Lefter; Olivia O' Mahony; Brian Sweeney; Aisling M Ryan
Journal:  Mov Disord Clin Pract       Date:  2020-10-28
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