Literature DB >> 27261689

Genetic Leukoencephalopathies in Adults.

Adeline Vanderver.   

Abstract

PURPOSE OF REVIEW: More than 100 heritable disorders can present with abnormal white matter on neuroimaging. While acquired disorders remain a more common cause of leukoencephalopathy in the adult than genetic causes, the clinician must remain aware of features that suggest a possible genetic etiology. RECENT
FINDINGS: The differential diagnosis of heritable white matter disorders in adults has been revolutionized by next-generation sequencing approaches and the recent identification of the molecular cause of a series of adult-onset disorders.
SUMMARY: The identification of a heritable etiology of white matter disease will often have important prognostic and family counseling implications. It is thus important to be aware of the most common hereditary disorders of the white matter and to know how to distinguish them from acquired disorders and how to approach their diagnosis.

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Year:  2016        PMID: 27261689      PMCID: PMC5617213          DOI: 10.1212/CON.0000000000000338

Source DB:  PubMed          Journal:  Continuum (Minneap Minn)        ISSN: 1080-2371


  44 in total

1.  MRI and CT in an autosomal-dominant, adult-onset leukodystrophy.

Authors:  M Bergui; G B Bradac; S Leombruni; G Vaula; G Quattrocolo
Journal:  Neuroradiology       Date:  1997-06       Impact factor: 2.804

2.  Neurotransmitter abnormalities and response to supplementation in SPG11.

Authors:  Adeline Vanderver; Davide Tonduti; Sarah Auerbach; Johanna L Schmidt; Sumit Parikh; Gordon C Gowans; Kelly E Jackson; Pamela L Brock; Marc Patterson; Michelle Nehrebecky; Rena Godfrey; Wadih M Zein; William Gahl; Camilo Toro
Journal:  Mol Genet Metab       Date:  2012-06-01       Impact factor: 4.797

3.  A new leukoencephalopathy with vanishing white matter.

Authors:  M S van der Knaap; P G Barth; F J Gabreëls; E Franzoni; J H Begeer; H Stroink; J J Rotteveel; J Valk
Journal:  Neurology       Date:  1997-04       Impact factor: 9.910

4.  Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.

Authors:  M S van der Knaap; V Ramesh; R Schiffmann; S Blaser; M Kyllerman; A Gholkar; D W Ellison; J P van der Voorn; S J M van Dooren; C Jakobs; F Barkhof; G S Salomons
Journal:  Neurology       Date:  2006-02-28       Impact factor: 9.910

5.  Autosomal dominant diffuse leukoencephalopathy with neuroaxonal spheroids.

Authors:  M S van der Knaap; S Naidu; B K Kleinschmidt-Demasters; W Kamphorst; H C Weinstein
Journal:  Neurology       Date:  2000-01-25       Impact factor: 9.910

6.  Glycogen branching enzyme deficiency in adult polyglucosan body disease.

Authors:  C Bruno; S Servidei; S Shanske; G Karpati; S Carpenter; D McKee; R J Barohn; M Hirano; Z Rifai; S DiMauro
Journal:  Ann Neurol       Date:  1993-01       Impact factor: 10.422

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.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family.

Authors:  G Sabbadini; A Francia; L Calandriello; C Di Biasi; G Trasimeni; G F Gualdi; G Palladini; M Manfredi; M Frontali
Journal:  Brain       Date:  1995-02       Impact factor: 13.501

9.  Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism.

Authors:  Hussein Daoud; Martine Tétreault; William Gibson; Kether Guerrero; Ana Cohen; Janina Gburek-Augustat; Matthis Synofzik; Bernard Brais; Cathy A Stevens; Rocio Sanchez-Carpintero; Cyril Goizet; Sakkubai Naidu; Adeline Vanderver; Geneviève Bernard
Journal:  J Med Genet       Date:  2013-01-25       Impact factor: 6.318

10.  Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity.

Authors:  Ryan J Taft; Adeline Vanderver; Richard J Leventer; Stephen A Damiani; Cas Simons; Sean M Grimmond; David Miller; Johanna Schmidt; Paul J Lockhart; Kate Pope; Kelin Ru; Joanna Crawford; Tena Rosser; Irenaeus F M de Coo; Monica Juneja; Ishwar C Verma; Prab Prabhakar; Susan Blaser; Julian Raiman; Petra J W Pouwels; Marianna R Bevova; Truus E M Abbink; Marjo S van der Knaap; Nicole I Wolf
Journal:  Am J Hum Genet       Date:  2013-05-02       Impact factor: 11.025

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  5 in total

1.  An adolescence-onset male leukoencephalopathy with remarkable cerebellar atrophy and novel compound heterozygous AARS2 gene mutations: a case report.

Authors:  Qing Dong; Ling Long; Yan-Yu Chang; Yan-Jun Lin; Mei Liu; Zheng-Qi Lu
Journal:  J Hum Genet       Date:  2018-04-17       Impact factor: 3.172

Review 2.  On the dynamic and even reversible nature of Leigh syndrome: Lessons from human imaging and mouse models.

Authors:  Melissa A Walker; Maria Miranda; Amanda Allred; Vamsi K Mootha
Journal:  Curr Opin Neurobiol       Date:  2021-10-14       Impact factor: 7.070

3.  Case Report: Mutation in AIMP2/P38, the Scaffold for the Multi-Trna Synthetase Complex, and Association With Progressive Neurodevelopmental Disorders.

Authors:  Mahta Mazaheri; Mahdie Yavari; Hadi Zare Marzouni; Angela Stufano; Piero Lovreglio; Simona S'Amore; Hamid Reza Jahantigh
Journal:  Front Genet       Date:  2022-01-24       Impact factor: 4.599

4.  The White Matter Rounds experience: The importance of a multidisciplinary network to accelerate the diagnostic process for adult patients with rare white matter disorders.

Authors:  Yu Tong Huang; Paul S Giacomini; Rami Massie; Sunita Venkateswaran; Anne-Marie Trudelle; Giulia Fadda; Maryam Sharifian-Dorche; Hayet Boudjani; Laurence Poliquin-Lasnier; Laura Airas; Alexander W Saveriano; Matthias Georg Ziller; Elka Miller; Claudia Martinez-Rios; Nagwa Wilson; Jorge Davila; Carolina Rush; Erin E Longbrake; Giulia Longoni; Gabrielle Macaron; Geneviève Bernard; Donatella Tampieri; Jack Antel; Bernard Brais; Roberta La Piana
Journal:  Front Neurol       Date:  2022-07-25       Impact factor: 4.086

5.  Natural History of Vanishing White Matter.

Authors:  Eline M C Hamilton; Hannemieke D W van der Lei; Gerre Vermeulen; Jan A M Gerver; Charles M Lourenço; Sakkubai Naidu; Hanna Mierzewska; Reinoud J B J Gemke; Henrica C W de Vet; Bernard M J Uitdehaag; Birgit I Lissenberg-Witte; Marjo S van der Knaap
Journal:  Ann Neurol       Date:  2018-09-06       Impact factor: 11.274

  5 in total

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