MRI in the mild type of mucopolysaccharidosis II (Hunter's syndrome)

被引:1
|
作者
Shinomiya, N
Nagayama, T
Fujioka, Y
Aoki, T
机构
关键词
Hunter's syndrome; mucopolysaccharidosis; magnetic resonance imaging; computed tomography; Virchow-Robin spaces;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report imaging findings in a 3-year-old boy with the typical mild type of Hunter's disease, MRI revealed multifocal large cyst- or spindle-like areas of increased and decreased signal in the white matter, including the corpus callosum on T1- and T2-weighted images, The white matter showed high signal on T2-weighted images, isointense with cerebrospinal fluid on all other pulse sequences. To our knowledge, these appearances have not been reported in this disorder, Deposition of mucopolysaccharide and/or glycolipid and increase in fluid content seem to be responsible.
引用
收藏
页码:483 / 485
页数:3
相关论文
共 50 条
  • [31] The reliability of death certification in patients dying with mucopolysaccharidosis type II (Hunter syndrome)
    Seshadri, D.
    Jones, S.
    Burt, K.
    Lavery, L.
    Wraith, J. E.
    [J]. CLINICAL GENETICS, 2011, 79 (06) : 599 - 600
  • [32] Enzyme replacement therapy in mucopolysaccharidosis type II (Hunter syndrome): a preliminary report
    Muenzer, J
    Lamsa, JC
    Garcia, A
    Dacosta, J
    Garcia, J
    Treco, DA
    [J]. ACTA PAEDIATRICA, 2002, 91 : 98 - 99
  • [33] Mucopolysaccharidosis type II (Hunter syndrome) in Thai children: Report of 16 cases
    Wasant, P.
    Liammongkolkul, S.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 : 154 - 154
  • [34] Expression studies of mutations underlying Taiwanese Hunter syndrome (mucopolysaccharidosis type II)
    Chang, JH
    Lin, SP
    Lin, SC
    Tseng, KL
    Li, CL
    Chuang, CK
    Lee-Chen, GJ
    [J]. HUMAN GENETICS, 2005, 116 (03) : 160 - 166
  • [35] Atypical clinical presentation of mucopolysaccharidosis type II (Hunter syndrome): A case report
    Shah G.S.
    Mahal T.
    Sharma S.
    [J]. Journal of Medical Case Reports, 4 (1)
  • [36] Expression studies of mutations underlying Taiwanese Hunter syndrome (mucopolysaccharidosis type II)
    Jui-Hung Chang
    Shuan-Pei Lin
    Shu-Chuan Lin
    Kai-Li Tseng
    Chia-Ling Li
    Chih-Kuang Chuang
    Guey-Jen Lee-Chen
    [J]. Human Genetics, 2005, 116 : 160 - 166
  • [37] Retroviral transduction and expansion of peripheral blood lymphocytes for the treatment of mucopolysaccharidosis type II, Hunter's syndrome
    Stroncek, DF
    Hubel, A
    Shankar, RA
    Burger, SR
    Pan, D
    McCullough, J
    Whitley, CB
    [J]. TRANSFUSION, 1999, 39 (04) : 343 - 350
  • [38] Diagnosis and therapy options in mucopolysaccharidosis II (Hunter syndrome)
    Giugliani, Roberto
    Brusius-Facchin, Ana Carolina
    Moura de Souza, Carolina Fischinger
    Civallero, Gabriel
    Burin, Maira
    Leistner-Segal, Sandra
    Baldo, Guilherme
    Vairo, Filippo
    [J]. EXPERT OPINION ON ORPHAN DRUGS, 2015, 3 (02): : 141 - 150
  • [39] Idursulfase desensitization in a child with Hunter syndrome (mucopolysaccharidosis II)
    Bustamante, Lucrecia L.
    Garavaglia, Luciano
    Garramone, Esteban, I
    Amartino, Hernan
    Parisi, Claudio A. S.
    [J]. ARCHIVOS ARGENTINOS DE PEDIATRIA, 2021, 119 (01): : E41 - E44
  • [40] The characterization of a murine model of mucopolysaccharidosis II (Hunter syndrome)
    Garcia, A. R.
    Pan, J.
    Lamsa, J. C.
    Muenzer, J.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2007, 30 (06) : 924 - 934