Literature DB >> 28087826

Comparison of brain MRI findings with language and motor function in the dystroglycanopathies.

Brianna N Brun1, Shelley R H Mockler1, Katie M Laubscher1, Carrie M Stephan1, Anne M Wallace1, Julia A Collison1, M Bridget Zimmerman1, William B Dobyns1, Katherine D Mathews2.   

Abstract

OBJECTIVE: To describe the spectrum of brain MRI findings in a cohort of individuals with dystroglycanopathies (DGs) and relate MRI results to function.
METHODS: All available brain MRIs done for clinical indications on individuals enrolled in a DG natural history study (NCT00313677) were reviewed. Reports were reviewed when MRI was not available. MRIs were categorized as follows: (1) cortical, brainstem, and cerebellar malformations; (2) cortical and cerebellar malformations; or (3) normal. Language development was assigned to 1 of 3 categories by a speech pathologist. Maximal motor function and presence of epilepsy were determined by history or examination.
RESULTS: Twenty-five MRIs and 9 reports were reviewed. The most common MRI abnormalities were cobblestone cortex or dysgyria with an anterior-posterior gradient and cerebellar hypoplasia. Seven individuals had MRIs in group 1, 8 in group 2, and 19 in group 3. Language was impaired in 100% of those in MRI groups 1 and 2, and degree of language impairment correlated with severity of imaging. Eighty-five percent of the whole group achieved independent walking, but only 33% did in group 1. Epilepsy was present in 8% of the cohort and rose to 37% of those with an abnormal MRI.
CONCLUSIONS: Developmental abnormalities of the brain such as cobblestone lissencephaly, cerebellar cysts, pontine hypoplasia, and brainstem bowing are hallmarks of DG and should prompt consideration of these diagnoses. Brain imaging in individuals with DG helps to predict outcomes, especially language development, aiding clinicians in prognostic counseling.
© 2017 American Academy of Neurology.

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Year:  2017        PMID: 28087826      PMCID: PMC5317381          DOI: 10.1212/WNL.0000000000003609

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


  32 in total

Review 1.  The neurogenetics of lissencephaly.

Authors:  W B Dobyns
Journal:  Neurol Clin       Date:  1989-02       Impact factor: 3.806

2.  Brain MRI abnormalities in muscular dystrophy due to FKRP mutations.

Authors:  Susana Quijano-Roy; Itxaso Martí-Carrera; Samira Makri; Michèle Mayer; Svetlana Maugenre; Pascale Richard; Carole Berard; Louis Viollet; Bruno Leheup; Pascale Guicheney; Jean-Marc Pinard; Brigitte Estournet; Robert Y Carlier
Journal:  Brain Dev       Date:  2005-12-20       Impact factor: 1.961

3.  A dystroglycan mutation associated with limb-girdle muscular dystrophy.

Authors:  Yuji Hara; Burcu Balci-Hayta; Takako Yoshida-Moriguchi; Motoi Kanagawa; Daniel Beltrán-Valero de Bernabé; Hülya Gündeşli; Tobias Willer; Jakob S Satz; Robert W Crawford; Steven J Burden; Stefan Kunz; Michael B A Oldstone; Alessio Accardi; Beril Talim; Francesco Muntoni; Haluk Topaloğlu; Pervin Dinçer; Kevin P Campbell
Journal:  N Engl J Med       Date:  2011-03-10       Impact factor: 91.245

4.  Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies.

Authors:  Louise Devisme; Céline Bouchet; Marie Gonzalès; Elisabeth Alanio; Anne Bazin; Bettina Bessières; Nicole Bigi; Patricia Blanchet; Dominique Bonneau; Maryse Bonnières; Martine Bucourt; Dominique Carles; Bénedicte Clarisse; Sophie Delahaye; Catherine Fallet-Bianco; Dominique Figarella-Branger; Dominique Gaillard; Bernard Gasser; Anne-Lise Delezoide; Fabien Guimiot; Madeleine Joubert; Nicole Laurent; Annie Laquerrière; Agnès Liprandi; Philippe Loget; Pascale Marcorelles; Jelena Martinovic; Francoise Menez; Sophie Patrier; Fanny Pelluard; Marie-José Perez; Caroline Rouleau; Stéphane Triau; Tania Attié-Bitach; Sandrine Vuillaumier-Barrot; Nathalie Seta; Férechté Encha-Razavi
Journal:  Brain       Date:  2012-02-09       Impact factor: 13.501

5.  Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations.

Authors:  Y Fukuyama; M Osawa; H Suzuki
Journal:  Brain Dev       Date:  1981       Impact factor: 1.961

6.  Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities.

Authors:  Farid Radmanesh; Ahmet Okay Caglayan; Jennifer L Silhavy; Cahide Yilmaz; Vincent Cantagrel; Tarek Omar; Başak Rosti; Hande Kaymakcalan; Stacey Gabriel; Mingfeng Li; Nenad Sestan; Kaya Bilguvar; William B Dobyns; Maha S Zaki; Murat Gunel; Joseph G Gleeson
Journal:  Am J Hum Genet       Date:  2013-03-07       Impact factor: 11.025

7.  A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan.

Authors:  Pervin Dinçer; Burcu Balci; Yeliz Yuva; Beril Talim; Martin Brockington; Deniz Dinçel; Silvia Torelli; Sue Brown; Gülsev Kale; Göknur Haliloglu; Filiz Ozbas Gerçeker; Rengül Cetin Atalay; Cengiz Yakicier; Cheryl Longman; Francesco Muntoni; Haluk Topaloglu
Journal:  Neuromuscul Disord       Date:  2003-12       Impact factor: 4.296

8.  Brain MR in Fukuyama congenital muscular dystrophy.

Authors:  N Aida; K Tamagawa; K Takada; A Yagishita; N Kobayashi; K Chikumaru; H Iwamoto
Journal:  AJNR Am J Neuroradiol       Date:  1996-04       Impact factor: 3.825

9.  Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations.

Authors:  Fatemeh Geranmayeh; Emma Clement; Lucy H Feng; Caroline Sewry; Judith Pagan; Rachael Mein; Stephen Abbs; Louise Brueton; Anne-Marie Childs; Heinz Jungbluth; Christian G De Goede; Bryan Lynch; Jean-Pierre Lin; Gabriel Chow; Carlos de Sousa; Olivia O'Mahony; Anirban Majumdar; Volker Straub; Katherine Bushby; Francesco Muntoni
Journal:  Neuromuscul Disord       Date:  2010-03-06       Impact factor: 4.296

10.  Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy.

Authors:  Caroline Godfrey; Diana Escolar; Martin Brockington; Emma M Clement; Rachael Mein; Cecilia Jimenez-Mallebrera; Silvia Torelli; Lucy Feng; Susan C Brown; Caroline A Sewry; Mary Rutherford; Yehuda Shapira; Stephen Abbs; Francesco Muntoni
Journal:  Ann Neurol       Date:  2006-11       Impact factor: 10.422

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  6 in total

1.  Lissencephaly: Expanded imaging and clinical classification.

Authors:  Nataliya Di Donato; Sara Chiari; Ghayda M Mirzaa; Kimberly Aldinger; Elena Parrini; Carissa Olds; A James Barkovich; Renzo Guerrini; William B Dobyns
Journal:  Am J Med Genet A       Date:  2017-04-25       Impact factor: 2.802

2.  TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.

Authors:  Laura V Vandervore; Rachel Schot; Chiara Milanese; Daphne J Smits; Esmee Kasteleijn; Andrew E Fry; Daniela T Pilz; Stefanie Brock; Esra Börklü-Yücel; Marco Post; Nadia Bahi-Buisson; María José Sánchez-Soler; Marjon van Slegtenhorst; Boris Keren; Alexandra Afenjar; Stephanie A Coury; Wen-Hann Tan; Renske Oegema; Linda S de Vries; Katherine A Fawcett; Peter G J Nikkels; Aida Bertoli-Avella; Amal Al Hashem; Abdulmalik A Alwabel; Kalthoum Tlili-Graiess; Stephanie Efthymiou; Faisal Zafar; Nuzhat Rana; Farah Bibi; Henry Houlden; Reza Maroofian; Richard E Person; Amy Crunk; Juliann M Savatt; Lisbeth Turner; Mohammad Doosti; Ehsan Ghayoor Karimiani; Nebal Waill Saadi; Javad Akhondian; Maarten H Lequin; Hülya Kayserili; Peter J van der Spek; Anna C Jansen; Johan M Kros; Robert M Verdijk; Nataša Jovanov Milošević; Maarten Fornerod; Pier Giorgio Mastroberardino; Grazia M S Mancini
Journal:  Am J Hum Genet       Date:  2019-11-14       Impact factor: 11.025

3.  Characteristic Cochlear Hypoplasia in Patients with Walker-Warburg Syndrome: A Radiologic Study of the Inner Ear in α-Dystroglycan-Related Muscular Disorders.

Authors:  G Talenti; C Robson; M S Severino; C A Alves; D Chitayat; H Dahmoush; L Smith; F Muntoni; S I Blaser; F D'Arco
Journal:  AJNR Am J Neuroradiol       Date:  2020-10-29       Impact factor: 3.825

Review 4.  Definitions and classification of malformations of cortical development: practical guidelines.

Authors:  Mariasavina Severino; Ana Filipa Geraldo; Norbert Utz; Domenico Tortora; Ivana Pogledic; Wlodzimierz Klonowski; Fabio Triulzi; Filippo Arrigoni; Kshitij Mankad; Richard J Leventer; Grazia M S Mancini; James A Barkovich; Maarten H Lequin; Andrea Rossi
Journal:  Brain       Date:  2020-10-01       Impact factor: 13.501

Review 5.  Towards Central Nervous System Involvement in Adults with Hereditary Myopathies.

Authors:  Jens Reimann; Cornelia Kornblum
Journal:  J Neuromuscul Dis       Date:  2020

Review 6.  International consensus recommendations on the diagnostic work-up for malformations of cortical development.

Authors:  Renske Oegema; Tahsin Stefan Barakat; Martina Wilke; Katrien Stouffs; Dina Amrom; Eleonora Aronica; Nadia Bahi-Buisson; Valerio Conti; Andrew E Fry; Tobias Geis; David Gomez Andres; Elena Parrini; Ivana Pogledic; Edith Said; Doriette Soler; Luis M Valor; Maha S Zaki; Ghayda Mirzaa; William B Dobyns; Orly Reiner; Renzo Guerrini; Daniela T Pilz; Ute Hehr; Richard J Leventer; Anna C Jansen; Grazia M S Mancini; Nataliya Di Donato
Journal:  Nat Rev Neurol       Date:  2020-09-07       Impact factor: 42.937

  6 in total

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