Nonprogressive familial leukoencephalopathy with porencephalic cyst and focal seizures

被引:0
作者
Blumkin, Lubov
Watemberg, Nathan
Lev, Dorit
Malinger, Gustavo
Luchman, Yehudit
Ben-Zeev, Bruria
Lerman-Sagie, Tally [1 ]
机构
[1] Wolfson Med Ctr, Pediat Neurol Unit, Metabol Neurogenet Clin, Prenatal Neurol Clin, IL-58100 Holon, Israel
[2] Wolfson Med Ctr, Prenatal Neurol Clin, Genet Inst, Metabol Neurogenet Clin, Holon, Israel
[3] Wolfson Med Ctr, Dept Radiol, Holon, Israel
[4] Chaim Sheba Med Ctr, Pediat Neurol Unit, Ramat Gan, Israel
关键词
D O I
10.1177/08830738060210021701
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Two siblings with a similar white-matter disease but different clinical symptoms are described. The first sibling suffers from nonprogressive spastic hemiparesis secondary to a congenital periventricular porencephalic cyst. Her brother has focal epilepsy. On magnetic resonance imaging, both patients show diffuse white-matter involvement predominantly of the posterior periventricular area. We suggest that this is a familial white-matter disorder with minimal symptoms and no progression in early childhood.
引用
收藏
页码:145 / 148
页数:4
相关论文
共 25 条
  • [1] Familial leukoencephalopathy in bipolar disorder
    Ahearn, EP
    Steffens, DC
    Cassidy, F
    Van Meter, SA
    Provenzale, JM
    Seldin, MF
    Weisler, RH
    Krishnan, KRR
    [J]. AMERICAN JOURNAL OF PSYCHIATRY, 1998, 155 (11) : 1605 - 1607
  • [2] Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews
    Ben-Zeev, B
    Levy-Nissenbaum, E
    Lahat, H
    Anikster, Y
    Shinar, Y
    Brand, N
    Gross-Tzur, V
    MacGregor, D
    Sidi, R
    Kleta, R
    Frydman, M
    Pras, E
    [J]. HUMAN GENETICS, 2002, 111 (02) : 214 - 218
  • [3] MRI and CT in an autosomal-dominant, adult-onset leukodystrophy
    Bergui, M
    Bradac, GB
    Leombruni, S
    Vaula, G
    Quattrocolo, G
    [J]. NEURORADIOLOGY, 1997, 39 (06) : 423 - 426
  • [4] Distribution of cranial MRI abnormalities in patients with symptomatic and subclinical CADASIL
    Coulthard, A
    Blank, SC
    Bushby, K
    Kalaria, RN
    Burn, DJ
    [J]. BRITISH JOURNAL OF RADIOLOGY, 2000, 73 (867) : 256 - 265
  • [5] The natural history of CADASIL - A pooled analysis of previously published cases
    Desmond, DW
    Moroney, JT
    Lynch, T
    Chan, S
    Chin, SS
    Mohr, JP
    [J]. STROKE, 1999, 30 (06) : 1230 - 1233
  • [6] Brain MRI features of congenital- and adult-form myotonic dystrophy type 1: case-control study
    Di Costanzo, A
    Di Salle, F
    Santoro, L
    Bonavita, V
    Tedeschi, G
    [J]. NEUROMUSCULAR DISORDERS, 2002, 12 (05) : 476 - 483
  • [7] FOLGI A, 2002, NEUROLOGY, V59, P1966
  • [8] Periventricular leukomalacia and epilepsy - Incidence and seizure pattern
    Gurses, C
    Gross, DW
    Andermann, F
    Bastos, A
    Dubeau, F
    Calay, M
    Eraksoy, M
    Bezci, S
    Andermann, E
    Melanson, D
    [J]. NEUROLOGY, 1999, 52 (02) : 341 - 345
  • [9] Update on genetic disorders affecting white matter
    Kaye, EM
    [J]. PEDIATRIC NEUROLOGY, 2001, 24 (01) : 11 - 24
  • [10] KOTORII S, 2001, CLIN NEUROL TOKYO, V41, P306