Literature DB >> 21920862

Neuroimaging features of neurodegeneration with brain iron accumulation.

M C Kruer1, N Boddaert, S A Schneider, H Houlden, K P Bhatia, A Gregory, J C Anderson, W D Rooney, P Hogarth, S J Hayflick.   

Abstract

NBIA characterizes a class of neurodegenerative diseases that feature a prominent extrapyramidal movement disorder, intellectual deterioration, and a characteristic deposition of iron in the basal ganglia. The diagnosis of NBIA is made on the basis of the combination of representative clinical features along with MR imaging evidence of iron accumulation. In many cases, confirmatory molecular genetic testing is now available as well. A number of new subtypes of NBIA have recently been described, with distinct neuroradiologic and clinical features. This article outlines the known subtypes of NBIA, delineates their clinical and radiographic features, and suggests an algorithm for evaluation.

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Year:  2011        PMID: 21920862      PMCID: PMC7966445          DOI: 10.3174/ajnr.A2677

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  38 in total

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2.  The "eye-of-the-tiger" sign is not pathognomonic of the PANK2 mutation.

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Journal:  Mov Disord       Date:  1999-01       Impact factor: 10.338

4.  A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome.

Authors:  B Zhou; S K Westaway; B Levinson; M A Johnson; J Gitschier; S J Hayflick
Journal:  Nat Genet       Date:  2001-08       Impact factor: 38.330

5.  Familial idiopathic brain calcification with autosomal dominant inheritance.

Authors:  M Kobari; S Nogawa; Y Sugimoto; Y Fukuuchi
Journal:  Neurology       Date:  1997-03       Impact factor: 9.910

6.  Novel histopathologic findings in molecularly-confirmed pantothenate kinase-associated neurodegeneration.

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Journal:  Brain       Date:  2011-04       Impact factor: 13.501

7.  Increased iron in the dentate nucleus of patients with Friedrich's ataxia.

Authors:  D Waldvogel; P van Gelderen; M Hallett
Journal:  Ann Neurol       Date:  1999-07       Impact factor: 10.422

8.  Multiple sclerosis and the accumulation of iron in the Basal Ganglia: quantitative assessment of brain iron using MRI t(2) relaxometry.

Authors:  A Burgetova; Z Seidl; J Krasensky; D Horakova; M Vaneckova
Journal:  Eur Neurol       Date:  2010-01-30       Impact factor: 1.710

9.  Intellectual and adaptive behaviour functioning in pantothenate kinase-associated neurodegeneration.

Authors:  K Freeman; A Gregory; A Turner; P Blasco; P Hogarth; S Hayflick
Journal:  J Intellect Disabil Res       Date:  2007-06

10.  ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation.

Authors:  Susanne A Schneider; Coro Paisan-Ruiz; Niall P Quinn; Andrew J Lees; Henry Houlden; John Hardy; Kailash P Bhatia
Journal:  Mov Disord       Date:  2010-06-15       Impact factor: 10.338

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  64 in total

1.  Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome.

Authors:  Mansoor C Abdulla; Anas M Alazami; Jemshad Alungal; Jassim M Koya; Mohthash Musambil
Journal:  J Genet       Date:  2015-09       Impact factor: 1.166

2.  FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

Authors:  Tim W Rattay; Tobias Lindig; Jonathan Baets; Katrien Smets; Tine Deconinck; Anne S Söhn; Konstanze Hörtnagel; Kathrin N Eckstein; Sarah Wiethoff; Jennifer Reichbauer; Marion Döbler-Neumann; Ingeborg Krägeloh-Mann; Michaela Auer-Grumbach; Barbara Plecko; Alexander Münchau; Bernd Wilken; Marc Janauschek; Anne-Katrin Giese; Jan L De Bleecker; Els Ortibus; Martine Debyser; Adolfo Lopez de Munain; Aurora Pujol; Maria Teresa Bassi; Maria Grazia D'Angelo; Peter De Jonghe; Stephan Züchner; Peter Bauer; Ludger Schöls; Rebecca Schüle
Journal:  Brain       Date:  2019-06-01       Impact factor: 13.501

Review 3.  Genetics of neurodegeneration with brain iron accumulation.

Authors:  Allison Gregory; Susan J Hayflick
Journal:  Curr Neurol Neurosci Rep       Date:  2011-06       Impact factor: 5.081

4.  De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood.

Authors:  Hirotomo Saitsu; Taki Nishimura; Kazuhiro Muramatsu; Hirofumi Kodera; Satoko Kumada; Kenji Sugai; Emi Kasai-Yoshida; Noriko Sawaura; Hiroya Nishida; Ai Hoshino; Fukiko Ryujin; Seiichiro Yoshioka; Kiyomi Nishiyama; Yukiko Kondo; Yoshinori Tsurusaki; Mitsuko Nakashima; Noriko Miyake; Hirokazu Arakawa; Mitsuhiro Kato; Noboru Mizushima; Naomichi Matsumoto
Journal:  Nat Genet       Date:  2013-02-24       Impact factor: 38.330

5.  Cortical pencil lining in neuroferritinopathy: a diagnostic clue.

Authors:  Amit Batla; Matthew E Adams; Roberto Erro; Christos Ganos; Bettina Balint; Niccolo E Mencacci; Kailash P Bhatia
Journal:  Neurology       Date:  2015-04-01       Impact factor: 9.910

6.  13-year diagnostic delay as cerebral palsy of an Iraqi patient with NBIA type 4.

Authors:  Ameer Shaker Hadi; Nebal Waill Saadi; Qusay Abed Fahad
Journal:  Neurol Clin Pract       Date:  2019-06

7.  WDR45 Mutation in Atypical Rett Syndrome with Brain Iron Accumulation.

Authors:  Sarah J Crisp; Esther Meyer; Allison Gregory; Hayley Archer; Susan Hayflick; Manju A Kurian; Rajith de Silva
Journal:  Mov Disord Clin Pract       Date:  2015-02-24

8.  Neurodegeneration with brain iron accumulation: A case report.

Authors:  Daniel Nassif; João Santos Pereira; Mariana Spitz; Cláudia Capitão; Alessandra Faria
Journal:  Dement Neuropsychol       Date:  2016 Apr-Jun

9.  Dysregulated iron metabolism in the choroid plexus in fragile X-associated tremor/ataxia syndrome.

Authors:  Jeanelle Ariza; Craig Steward; Flora Rueckert; Matt Widdison; Robert Coffman; Atiyeh Afjei; Stephen C Noctor; Randi Hagerman; Paul Hagerman; Verónica Martínez-Cerdeño
Journal:  Brain Res       Date:  2014-12-09       Impact factor: 3.252

10.  Lessons from a pair of siblings with BPAN.

Authors:  Yuri A Zarate; Julie R Jones; Melanie A Jones; Francisca Millan; Jane Juusola; Annette Vertino-Bell; G Bradley Schaefer; Michael C Kruer
Journal:  Eur J Hum Genet       Date:  2015-11-18       Impact factor: 4.246

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