Literature DB >> 17620549

Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.

M S van der Knaap1, T Linnankivi, A Paetau, A Feigenbaum, K Wakusawa, K Haginoya, W Köhler, M Henneke, A Dinopoulos, P Grattan-Smith, K Brockmann, R Schiffmann, S Blaser.   

Abstract

BACKGROUND AND
OBJECTIVE: Hypomyelination with atrophy of the basal ganglia and cerebellum is a recently defined disorder. Only a few patients have been described. We report on 11 additional patients and new MRI findings and provide histopathologic confirmation of the MRI interpretation.
METHODS: We reviewed the patients' clinical history and present findings. We scored the MRI abnormalities. The histopathology of one patient was re-examined.
RESULTS: The patients' early psychomotor development was normal or delayed, followed by increasing extrapyramidal movement abnormalities, ataxia, and spasticity. Mental capacities were variably affected. MRI showed hypomyelination with, on follow-up, evidence of further myelin loss and variable white matter atrophy. The putamen was small or, more often, absent; the head of the caudate nucleus was decreased in size. In contrast, the thalamus and globus pallidus remained normal. Cerebellar atrophy was invariably present. Histopathology confirmed the myelin deficiency, probably related to both lack of deposition and low-grade further loss. The degeneration of putamen was subtotal. The cerebellar cortex was affected, particularly the granular layer.
CONCLUSION: Hypomyelination with atrophy of the basal ganglia and cerebellum is a syndrome diagnosed by distinctive MRI findings. Histopathology confirms hypomyelination, low-grade further myelin loss, subtotal degeneration of the putamen, and cerebellar cortical atrophy. All known patients are sporadic, and the mode of inheritance is unclear.

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Mesh:

Year:  2007        PMID: 17620549     DOI: 10.1212/01.wnl.0000265592.74483.a6

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  18 in total

1.  Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings.

Authors:  Anna Sagnelli; Stefania Magri; Laura Farina; Luisa Chiapparini; Giorgio Marotta; Davide Tonduti; Monica Consonni; Graziana Maria Scigliuolo; Riccardo Benti; Davide Pareyson; Franco Taroni; Ettore Salsano; Daniela Di Bella
Journal:  J Neurol       Date:  2016-01-25       Impact factor: 4.849

2.  Hypomyelinating leukoencephalopathy.

Authors:  Riaz A Syed
Journal:  Sultan Qaboos Univ Med J       Date:  2013-02-27

3.  Neurochemical Metabolomics Reveals Disruption to Sphingolipid Metabolism Following Chronic Haloperidol Administration.

Authors:  Joseph L McClay; Sarah A Vunck; Angela M Batman; James J Crowley; Robert E Vann; Patrick M Beardsley; Edwin J van den Oord
Journal:  J Neuroimmune Pharmacol       Date:  2015-04-08       Impact factor: 4.147

4.  Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation.

Authors:  Eline M Hamilton; Emiel Polder; Adeline Vanderver; Sakkubai Naidu; Raphael Schiffmann; Kate Fisher; Ana Boban Raguž; Luba Blumkin; Carola G M van Berkel; Quinten Waisfisz; Cas Simons; Ryan J Taft; Truus E M Abbink; Nicole I Wolf; Marjo S van der Knaap
Journal:  Brain       Date:  2014-04-30       Impact factor: 13.501

5.  Invited article: an MRI-based approach to the diagnosis of white matter disorders.

Authors:  Raphael Schiffmann; Marjo S van der Knaap
Journal:  Neurology       Date:  2009-02-24       Impact factor: 9.910

6.  Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene.

Authors:  Lubov Blumkin; Ayelet Halevy; Dominique Ben-Ami-Raichman; Dvir Dahari; Ami Haviv; Cohen Sarit; Dorit Lev; Marjo S van der Knaap; Tally Lerman-Sagie; Esther Leshinsky-Silver
Journal:  Neurogenetics       Date:  2014-02-14       Impact factor: 2.660

7.  A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum.

Authors:  Cas Simons; Nicole I Wolf; Nathan McNeil; Ljubica Caldovic; Joseph M Devaney; Asako Takanohashi; Joanna Crawford; Kelin Ru; Sean M Grimmond; David Miller; Davide Tonduti; Johanna L Schmidt; Robert S Chudnow; Rudy van Coster; Lieven Lagae; Jill Kisler; Jürgen Sperner; Marjo S van der Knaap; Raphael Schiffmann; Ryan J Taft; Adeline Vanderver
Journal:  Am J Hum Genet       Date:  2013-04-11       Impact factor: 11.025

8.  TUBB4A de novo mutations cause isolated hypomyelination.

Authors:  Amy Pizzino; Tyler Mark Pierson; Yiran Guo; Guy Helman; Sebastian Fortini; Kether Guerrero; Sulagna Saitta; Jennifer Louise Patrick Murphy; Quasar Padiath; Yi Xie; Hakon Hakonarson; Xun Xu; Tara Funari; Michelle Fox; Ryan J Taft; Marjo S van der Knaap; Geneviève Bernard; Raphael Schiffmann; Cas Simons; Adeline Vanderver
Journal:  Neurology       Date:  2014-08-01       Impact factor: 9.910

9.  Clinical exome sequencing identifies a novel TUBB4A mutation in a child with static hypomyelinating leukodystrophy.

Authors:  Shawn M Purnell; Steven B Bleyl; Joshua L Bonkowsky
Journal:  Pediatr Neurol       Date:  2014-02-10       Impact factor: 3.372

Review 10.  Genes involved in leukodystrophies: a glance at glial functions.

Authors:  Odile Boespflug-Tanguy; Pierre Labauge; Anne Fogli; Catherine Vaurs-Barriere
Journal:  Curr Neurol Neurosci Rep       Date:  2008-05       Impact factor: 5.081

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