MRI in 3-methylglutaconic aciduria type 1

被引:8
作者
Arbelaez, A [1 ]
Castillo, M [1 ]
Stone, J [1 ]
机构
[1] Univ N Carolina, Sch Med, Dept Radiol, Chapel Hill, NC 27599 USA
关键词
3-methyl glutaconic aciduria; magnetic resonance imaging;
D O I
10.1007/s002340050871
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
MRI in a young child with 3-methylglutaconic aciduria type 1 showed signal abnormalities in the basal ganglia which progressed despite successful treatment.
引用
收藏
页码:941 / 942
页数:2
相关论文
共 5 条
  • [1] 3-METHYLGLUTACONIC ACIDURIA - A MARKER FOR AS YET UNSPECIFIED DISORDERS AND THE RELEVANCE OF PRENATAL-DIAGNOSIS IN A NEW TYPE (TYPE-4)
    CHITAYAT, D
    CHEMKE, J
    GIBSON, KM
    MAMER, OA
    KRONICK, JB
    MCGILL, JJ
    ROSENBLATT, B
    SWEETMAN, L
    SCRIVER, CR
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1992, 15 (02) : 204 - 212
  • [2] PHENOTYPIC HETEROGENEITY IN THE SYNDROMES OF 3-METHYLGLUTACONIC ACIDURIA
    GIBSON, KM
    SHERWOOD, WG
    HOFFMANN, GF
    STUMPF, DA
    DIANZANI, I
    SCHUTGENS, RBH
    BARTH, PG
    WEISMANN, U
    BACHMANN, C
    SCHRYNEMACKERSPITANCE, P
    VERLOES, A
    NARISAWA, K
    MINO, M
    OHYA, N
    KELLEY, RI
    [J]. JOURNAL OF PEDIATRICS, 1991, 118 (06) : 885 - 890
  • [3] Variable clinical presentation in three patients with 3-methylglutaconyl-coenzyme A hydratase deficiency
    Gibson, KM
    Wappner, RS
    Jooste, S
    Erasmus, E
    Mienie, LJ
    Gerlo, E
    Desprechins, B
    De Meirleir, L
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1998, 21 (06) : 631 - 638
  • [4] DEFICIENCY OF 3-METHYLGLUTACONYL-COENZYME-A HYDRATASE IN 2 SIBLINGS WITH 3-METHYLGLUTACONIC ACIDURIA
    NARISAWA, K
    GIBSON, KM
    SWEETMAN, L
    NYHAN, WL
    DURAN, M
    WADMAN, SK
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (04) : 1148 - 1152
  • [5] ZEHARIA A, 1992, PEDIATRICS, V89, P1080