Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.

نویسندگان

  • Xavier Ayrignac
  • Clarisse Carra-Dalliere
  • Nicolas Menjot de Champfleur
  • Christian Denier
  • Patrick Aubourg
  • Celine Bellesme
  • Giovanni Castelnovo
  • Jean Pelletier
  • Bertrand Audoin
  • Elsa Kaphan
  • Jerome de Seze
  • Nicolas Collongues
  • Frederic Blanc
  • Jean-Baptiste Chanson
  • Eloi Magnin
  • Eric Berger
  • Sandra Vukusic
  • Francoise Durand-Dubief
  • Jean-Philippe Camdessanche
  • Mickael Cohen
  • Christine Lebrun-Frenay
  • David Brassat
  • Michel Clanet
  • Patrick Vermersch
  • Helene Zephir
  • Olivier Outteryck
  • Sandrine Wiertlewski
  • David-Axel Laplaud
  • Jean-Christophe Ouallet
  • Bruno Brochet
  • Cyril Goizet
  • Marc Debouverie
  • Sophie Pittion
  • Gilles Edan
  • Véronique Deburghgraeve
  • Emmanuelle Le Page
  • Christophe Verny
  • Patrizia Amati-Bonneau
  • Dominique Bonneau
  • Didier Hannequin
  • Lucie Guyant-Maréchal
  • Nathalie Derache
  • Gilles Louis Defer
  • Thibault Moreau
  • Maurice Giroud
  • Anne Marie Guennoc
  • Pierre Clavelou
  • Frédérique Taithe
  • Stephane Mathis
  • Jean-Philippe Neau
  • Laurent Magy
  • Jean Louis Devoize
  • Marc Bataillard
  • Julien Masliah-Planchon
  • Imen Dorboz
  • Elisabeth Tournier-Lasserve
  • Thierry Levade
  • Odile Boespflug Tanguy
  • Pierre Labauge
چکیده

Inherited white matter diseases are rare and heterogeneous disorders usually encountered in infancy. Adult-onset forms are increasingly recognized. Our objectives were to determine relative frequencies of genetic leukoencephalopathies in a cohort of adult-onset patients and to evaluate the effectiveness of a systematic diagnostic approach. Inclusion criteria of this retrospective study were: (i) symmetrical involvement of white matter on the first available brain MRI; (ii) age of onset above 16 years. Patients with acquired diseases were excluded. Magnetic resonance imaging analysis identified three groups (vascular, cavitary and non-vascular/non-cavitary) in which distinct genetic and/or biochemical testing were realized. One hundred and fifty-four patients (male/female = 60/94) with adult-onset leukoencephalopathies were identified. Mean age of onset was 38.6 years. In the vascular group, 41/55 patients (75%) finally had a diagnosis [including CADASIL (cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy, n = 32) and COL4A1 mutation, n = 7]. In the cavitary group, 13/17 (76%) patients had a diagnosis of EIF2B-related disorder. In the third group (n = 82), a systematic biological screening allowed a diagnosis in 23 patients (28%) and oriented direct genetic screening identified 21 additional diseases (25.6%). Adult-onset genetic leukoencephalopathies are a rare but probably underestimated entity. Our study confirms the use of a magnetic resonance imaging-based classification with a final diagnosis rate of 64% (98/154) cases.

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عنوان ژورنال:
  • Brain : a journal of neurology

دوره 138 Pt 2  شماره 

صفحات  -

تاریخ انتشار 2015