Literature DB >> 8909455

Adult-onset neurodegenerative disorder due to proteolipid protein gene mutation in the mother of a man with Pelizaeus-Merzbacher disease.

M A Nance1, S Boyadjiev, V M Pratt, S Taylor, M E Hodes, S R Dlouhy.   

Abstract

A 23-year-old man with Pelizaeus-Merzbacher disease had a novel mutation, C344A (Thr115Lys), in exon 3 of the proteolipid protein gene (PLP) His mother, heterozygous for the mutation, developed progressive personality change and a gait disorder in her mid-20s. Her MRI at age 53 showed a diffuse severe leukodystrophy. This report extends the phenotypic range of disease due to PLP gene mutations to include adult-onset dementia in females.

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Year:  1996        PMID: 8909455     DOI: 10.1212/wnl.47.5.1333

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


  10 in total

Review 1.  PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2.

Authors:  Ken Inoue
Journal:  Neurogenetics       Date:  2004-12-31       Impact factor: 2.660

2.  Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathy.

Authors:  Michael E Shy; Grace Hobson; Manisha Jain; Odile Boespflug-Tanguy; James Garbern; Karen Sperle; Wen Li; Alex Gow; Diana Rodriguez; Enrico Bertini; Pedro Mancias; Karen Krajewski; Richard Lewis; John Kamholz
Journal:  Ann Neurol       Date:  2003-03       Impact factor: 10.422

3.  MR characteristics and neuropathology in adult-onset autosomal dominant leukodystrophy with autonomic symptoms.

Authors:  A Melberg; L Hallberg; H Kalimo; R Raininko
Journal:  AJNR Am J Neuroradiol       Date:  2006-04       Impact factor: 3.825

4.  Insertion of mutant proteolipid protein results in missorting of myelin proteins.

Authors:  Catherine Vaurs-Barriere; Kondi Wong; Thais D Weibel; Mones Abu-Asab; Michael D Weiss; Christine R Kaneski; Tong-Hui Mixon; Simona Bonavita; Isabelle Creveaux; John D Heiss; Maria Tsokos; Ehud Goldin; Richard H Quarles; Odile Boespflug-Tanguy; Raphael Schiffmann
Journal:  Ann Neurol       Date:  2003-12       Impact factor: 10.422

5.  Altered PLP1 splicing causes hypomyelination of early myelinating structures.

Authors:  Sietske H Kevelam; Jennifer R Taube; Rosalina M L van Spaendonk; Enrico Bertini; Karen Sperle; Mark Tarnopolsky; Davide Tonduti; Enza Maria Valente; Lorena Travaglini; Erik A Sistermans; Geneviève Bernard; Coriene E Catsman-Berrevoets; Clara D M van Karnebeek; John R Østergaard; Richard L Friederich; Mahmoud Fawzi Elsaid; Jolanda H Schieving; Maja Tarailo-Graovac; Simona Orcesi; Marjan E Steenweg; Carola G M van Berkel; Quinten Waisfisz; Truus E M Abbink; Marjo S van der Knaap; Grace M Hobson; Nicole I Wolf
Journal:  Ann Clin Transl Neurol       Date:  2015-05-01       Impact factor: 4.511

6.  Transcriptional mutagenesis reduces splicing fidelity in mammalian cells.

Authors:  João A Paredes; Monika Ezerskyte; Matteo Bottai; Kristian Dreij
Journal:  Nucleic Acids Res       Date:  2017-06-20       Impact factor: 16.971

7.  Morpholino Antisense Oligomers as a Potential Therapeutic Option for the Correction of Alternative Splicing in PMD, SPG2, and HEMS.

Authors:  Stephanie Tantzer; Karen Sperle; Kaitlin Kenaley; Jennifer Taube; Grace M Hobson
Journal:  Mol Ther Nucleic Acids       Date:  2018-07-05       Impact factor: 8.886

Review 8.  Genetic architecture of common non-Alzheimer's disease dementias.

Authors:  Rita Guerreiro; Elizabeth Gibbons; Miguel Tábuas-Pereira; Celia Kun-Rodrigues; Gustavo C Santo; Jose Bras
Journal:  Neurobiol Dis       Date:  2020-05-19       Impact factor: 5.996

9.  Genotype-phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus-merzbacher disease.

Authors:  Ruoyu Duan; Haoran Ji; Huifang Yan; Junyu Wang; Yu Zhang; Qian Zhang; Dongxiao Li; Binbin Cao; Qiang Gu; Ye Wu; Yuwu Jiang; Ming Li; Jingmin Wang
Journal:  Orphanet J Rare Dis       Date:  2022-03-28       Impact factor: 4.123

Review 10.  Mutation of Proteolipid Protein 1 Gene: From Severe Hypomyelinating Leukodystrophy to Inherited Spastic Paraplegia.

Authors:  Guy Khalaf; Claudia Mattern; Mélina Begou; Odile Boespflug-Tanguy; Charbel Massaad; Liliane Massaad-Massade
Journal:  Biomedicines       Date:  2022-07-15
  10 in total

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