Literature DB >> 2611559

Psychiatric features of adult GM2 gangliosidosis.

J Streifler1, M Golomb, N Gadoth.   

Abstract

The report describes three unrelated Ashkenazi Jewish women with adult GM2 gangliosidosis in whom mental symptoms were prominent, mimicking different psychiatric disorders, and thus delaying accurate diagnosis.

Entities:  

Mesh：

Year:  1989        PMID： 2611559     DOI： 10.1192/bjp.155.3.410

Source DB:  PubMed          Journal:  Br J Psychiatry        ISSN： 0007-1250            Impact factor:   9.319


  4 in total

Review 1.  Juvenile Sandhoff disease--nine new cases and a review of the literature.

Authors:  C J Hendriksz; P C Corry; J E Wraith; G T N Besley; A Cooper; C D Ferrie
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

2.  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

3.  Pontocerebellar atrophy is the hallmark neuroradiological finding in late-onset Tay-Sachs disease.

Authors:  Jitka Májovská; Anita Hennig; Igor Nestrasil; Susanne A Schneider; Helena Jahnová; Manuela Vaněčková; Martin Magner; Petr Dušek
Journal:  Neurol Sci       Date:  2021-11-20       Impact factor: 3.830

Review 4.  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
  4 in total

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