Leukodystrophies Classification, Diagnosis, and Treatment

被引:67
作者
Costello, Daniel J. [1 ]
Eichler, April F. [2 ]
Eichler, Florian S. [1 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Stephen E & Catherine Pappas Ctr Neurooncol, Boston, MA 02114 USA
关键词
leukodystrophy; X-linked adrenoleukodystrophy; metachromatic leukodystrophy; vanishing white matter disease; Alexander disease; Krabbe disease; magnetic resonance imaging; VANISHING WHITE-MATTER; GLOBOID-CELL LEUKODYSTROPHY; ADULT METACHROMATIC LEUKODYSTROPHY; X-LINKED ADRENOLEUKODYSTROPHY; PROTEIN GENE MUTATION; MEGALENCEPHALIC LEUKOENCEPHALOPATHY; SUBCORTICAL CYSTS; KRABBE-DISEASE; ONSET LEUKOENCEPHALOPATHY; TRANSPLANTATION;
D O I
10.1097/NRL.0b013e3181b287c8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The leukodystrophies are a heterogeneous group of diseases, which primarily affect white matter. Symptomatic patients are frequently misdiagnosed and the leukodystrophies are collectively under recognized. However, with ongoing research and increased availability of neuroimaging, our understanding of these diseases is increasing at a steady rate. Recent advances in the diagnosis and treatment of certain forms of leukodystrophy should prompt increased awareness of these diseases in clinical practice. Review Summary: The clinical features, pathophysiology, and therapeutic approach to these diseases are described. Particular emphasis is placed on genetic and pathophysiologic mechanisms, imaging patterns, screening of other family members and, where available, treatment options and resources, Conclusions: With more widespread use of neuroimaging, both pediatric and adult neurologists will increasingly be confronted with white matter disorders. Neurologists should have an approach to the recognition, diagnosis, and management of white matter diseases in general and the leukodystrophies in specific.
引用
收藏
页码:319 / 328
页数:10
相关论文
共 69 条
[61]  
van der Knaap MS, 2001, AM J NEURORADIOL, V22, P541
[62]   Vanishing white matter disease [J].
van der Knapp, MS ;
Scheper, GCS ;
Pronk, JC .
LANCET NEUROLOGY, 2006, 5 (05) :413-423
[63]   The life and death of Oligodendrocytes in vanishing white matter disease [J].
Van Haren, K ;
van der Voorn, JP ;
Peterson, DR ;
van der Knaap, MS ;
Powers, JM .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2004, 63 (06) :618-630
[64]   LEUKOENCEPHALOPATHY WITH SWELLING AND A DISCREPANTLY MILD CLINICAL COURSE IN 8 CHILDREN [J].
VANDERKNAAP, MS ;
BARTH, PG ;
STROINK, H ;
VANNIEUWENHUIZEN, O ;
ARTS, WFM ;
HOOGENRAAD, F ;
VALK, J .
ANNALS OF NEUROLOGY, 1995, 37 (03) :324-334
[65]   GLOBOID-CELL LEUKODYSTROPHY - A FAMILY WITH BOTH LATE-INFANTILE AND ADULT TYPE [J].
VERDRU, P ;
LAMMENS, M ;
DOM, R ;
VANELSEN, A ;
CARTON, H .
NEUROLOGY, 1991, 41 (09) :1382-1384
[66]   ADULT METACHROMATIC LEUKODYSTROPHY - VALUE OF COMPUTED TOMOGRAPHIC SCANNING AND MAGNETIC-RESONANCE-IMAGING OF THE BRAIN [J].
WALTZ, G ;
HARIK, SI ;
KAUFMAN, B .
ARCHIVES OF NEUROLOGY, 1987, 44 (02) :225-227
[67]   Primary progressive multiple sclerosis as a phenotype of a PLP1 gene mutation [J].
Warshawsky, I ;
Rudick, RA ;
Staugaitis, SM ;
Natowicz, MR .
ANNALS OF NEUROLOGY, 2005, 58 (03) :470-473
[68]   Krabbe disease: Genetic aspects and progress toward therapy [J].
Wenger, DA ;
Rafi, MA ;
Luzi, P ;
Datto, J ;
Costantino-Ceccarini, E .
MOLECULAR GENETICS AND METABOLISM, 2000, 70 (01) :1-9
[69]  
Wenger DA SK., 2001, The metabolic and molecular bases of inherited disease, V8, P3669