Literature DB >> 32223977

Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literature.

Chiara Benzoni1, Domenico Aquino2, Daniela Di Bella3, Elisa Sarto3, Marco Moscatelli2, Davide Pareyson1, Franco Taroni3, Ettore Salsano4.   

Abstract

Alexander disease (ALXDRD) is a rare astrocytic leukodystrophy caused by GFAP mutations. The adult-onset (AO) variant is usually characterized by gradual onset of spastic ataxia and bulbar symptoms with slowly progressive course. We report two AO-ALXDRD cases with rapid worsening after minor head trauma. In one of them, the only post-traumatic neuroimaging change was revealed by diffusion tensor imaging study. Our observations support the link between head trauma and ALXDRD progression, and suggest that this progression may be ascribed to microstructural changes. Clinicians should inform ALXDRD patients to minimize the risk of head trauma.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Alexander disease; Leukoencephalopathies; Nervous system trauma

Year:  2020        PMID: 32223977     DOI: 10.1016/j.jocn.2020.03.033

Source DB:  PubMed          Journal:  J Clin Neurosci        ISSN: 0967-5868            Impact factor:   1.961


  3 in total

1.  A novel in-frame GFAP p.E138_L148del mutation in Type II Alexander disease with atypical phenotypes.

Authors:  You-Ri Kang; So-Hyun Lee; Ni-Hsuan Lin; Seung-Jin Lee; Ai-Wen Yang; Gopalakrishnan Chandrasekaran; Kyung Wook Kang; Mi Sun Jin; Myeong-Kyu Kim; Ming-Der Perng; Seok-Yong Choi; Tai-Seung Nam
Journal:  Eur J Hum Genet       Date:  2022-03-04       Impact factor: 5.351

2.  Adult-Onset Alexander Disease: New Causal Sequence Variant in the GFAP Gene.

Authors:  Tsepo Goerttler; Letizia Zanetti; Maria Regoni; Karl Egger; Elias Kellner; Cornelius Deuschl; Christoph Kleinschnitz; Jenny Sassone; Stephan Klebe
Journal:  Neurol Genet       Date:  2022-05-20

Review 3.  Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing.

Authors:  Katayoun Heshmatzad; Niloofar Naderi; Tannaz Masoumi; Hamidreza Pouraliakbar; Samira Kalayinia
Journal:  Eur J Med Res       Date:  2022-09-10       Impact factor: 4.981

  3 in total

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