Literature DB >> 16417854

Diagnostic approach to cerebellar disease in children.

Stefano D'Arrigo1, Lucia Viganò, Maria Grazia Bruzzone, Michela Marzaroli, Ioannis Nikas, Daria Riva, Chiara Pantaleoni.   

Abstract

We reviewed the clinical records of 51 extensively investigated pediatric patients with structural abnormalities of the cerebellum as revealed by magnetic resonance imaging (MRI). Ten had hypoplasia of the vermis, 21 had hypoplasia of the vermis and cerebellar hemispheres, 2 had pontocerebellar hypoplasia, and 18 had progressive cerebellar atrophy. A clear diagnosis was reached in 37 (72.5%). Initial characterization of the cerebellar alterations by MRI separated hypoplastic from atrophic cases and confirmed MRI as an essential preliminary means for distinguishing malformations from metabolic-degenerative conditions. However, the diagnostic possibilities are so numerous that it is not feasible to propose a standardized diagnostic protocol for pediatric patients with an altered cerebellum. Subsequent investigations should be suggested by the neuroradiologic and clinical peculiarities of each case.

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Year:  2005        PMID: 16417854     DOI: 10.1177/08830738050200110101

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  7 in total

1.  Diagnostic approach to childhood-onset cerebellar atrophy: a 10-year retrospective study of 300 patients.

Authors:  Almundher Al-Maawali; Susan Blaser; Grace Yoon
Journal:  J Child Neurol       Date:  2012-07-04       Impact factor: 1.987

2.  Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy.

Authors:  Laurence Gauquelin; Taila Hartley; Mark Tarnopolsky; David A Dyment; Bernard Brais; Michael T Geraghty; Martine Tétreault; Sohnee Ahmed; Samantha Rojas; Karine Choquet; Jacek Majewski; François Bernier; Allan Micheil Innes; Guy Rouleau; Oksana Suchowersky; Kym M Boycott; Grace Yoon
Journal:  Mov Disord Clin Pract       Date:  2020-09-29

3.  How accurately does current fetal imaging identify posterior fossa anomalies?

Authors:  Catherine Limperopoulos; Richard L Robertson; Omar S Khwaja; Caroline D Robson; Judy A Estroff; Carole Barnewolt; Deborah Levine; Donna Morash; Luanne Nemes; Linda Zaccagnini; Adré J du Plessis
Journal:  AJR Am J Roentgenol       Date:  2008-06       Impact factor: 3.959

4.  Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome.

Authors:  Anna C Thomas; Hywel Williams; Núria Setó-Salvia; Chiara Bacchelli; Dagan Jenkins; Mary O'Sullivan; Konstantinos Mengrelis; Miho Ishida; Louise Ocaka; Estelle Chanudet; Chela James; Francesco Lescai; Glenn Anderson; Deborah Morrogh; Mina Ryten; Andrew J Duncan; Yun Jin Pai; Jorge M Saraiva; Fabiana Ramos; Bernadette Farren; Dawn Saunders; Bertrand Vernay; Paul Gissen; Anna Straatmaan-Iwanowska; Frank Baas; Nicholas W Wood; Joshua Hersheson; Henry Houlden; Jane Hurst; Richard Scott; Maria Bitner-Glindzicz; Gudrun E Moore; Sérgio B Sousa; Philip Stanier
Journal:  Am J Hum Genet       Date:  2014-11-06       Impact factor: 11.025

5.  Brain imaging features of children with Hoyeraal-Hreidarsson syndrome.

Authors:  Ming-Jie Zhang; Ya-Xian Cao; Hui-Ying Wu; He-Hong Li
Journal:  Brain Behav       Date:  2021-03-18       Impact factor: 2.708

6.  The natural history of ataxia-telangiectasia (A-T): A systematic review.

Authors:  Emily Petley; Alexander Yule; Shaun Alexander; Shalini Ojha; William P Whitehouse
Journal:  PLoS One       Date:  2022-03-15       Impact factor: 3.752

7.  Midbrain-hindbrain malformations in patients with malformations of cortical development and epilepsy: a series of 220 patients.

Authors:  Giorgi Kuchukhidze; Florian Koppelstaetter; Iris Unterberger; Judith Dobesberger; Gerald Walser; Julia Höfler; Laura Zamarian; Edda Haberlandt; Kevin Rostasy; Martin Ortler; Thomas Czech; Martha Feucht; Gerhard Bauer; Margarete Delazer; Stephan Felber; Eugen Trinka
Journal:  Epilepsy Res       Date:  2013-06-27       Impact factor: 3.045

  7 in total

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