Literature DB >> 15944912

Hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC). Report of a new case.

S Mercimek-Mahmutoglu1, M S van der Knaap, I Baric, D Prayer, S Stoeckler-Ipsiroglu.   

Abstract

Hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC) syndrome is a new neurodegenerative entity, which was first described by van der Knaap in 2002 in 7 patients aged from 2 months to 2 years. We describe a new, 42-month-old female patient who developed progressive dystonia, spasticity and oculogyric eye movements since the age of 3 months. The diagnosis was made by characteristic MRI findings including supratentorial hypomyelination and progressive atrophy of basal ganglia and cerebellum. Oculogyric eye movements have not been described in patients with H-ABC syndrome before. When compared with the normal age-related myelination patterns, the degree of hypomyelination increased progressively over the time course of 32 months, indicating arrest but not loss of myelination. The H-ABC syndrome adds to the differential diagnosis of progressive pyramidal and extrapyramidal movement disorders and to the increasing number of genetically determined hypomyelination syndromes.

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Year:  2005        PMID: 15944912     DOI: 10.1055/s-2005-865715

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  5 in total

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

2.  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

Review 3.  Cerebral folate deficiency.

Authors:  Keith Hyland; John Shoffner; Simon J Heales
Journal:  J Inherit Metab Dis       Date:  2010-07-29       Impact factor: 4.982

4.  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

5.  Longitudinal Evaluation of Cerebellar Signs of H-ABC Tubulinopathy in a Patient and in the taiep Model.

Authors:  Milvia Alata; Arturo González-Vega; Valeria Piazza; Anke Kleinert-Altamirano; Carmen Cortes; Juan C Ahumada-Juárez; Jose R Eguibar; Alejandra López-Juárez; Victor H Hernandez
Journal:  Front Neurol       Date:  2021-07-14       Impact factor: 4.003

  5 in total

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