Skeletal dysplasia and myelopathy in congenital disorder of glycosylation type IA

被引:13
|
作者
van Westrum, SMS
Nederkoorn, PJ
Schuurman, PR
Vulsma, T
Duran, M
Poll-The, BT
机构
[1] Univ Amsterdam, Acad Med Ctr, Div Pediat Neurol, Dept Pediat, NL-1100 DD Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Neurosurg, NL-1100 DD Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Lab Genet Metab Dis, NL-1100 DD Amsterdam, Netherlands
来源
JOURNAL OF PEDIATRICS | 2006年 / 148卷 / 01期
关键词
D O I
10.1016/j.jpeds.2005.08.048
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We report on a boy with a congenital disorder of glycosylation (CDG) la and a severe narrowing of the spinal canal caused by atlantoaxial subluxation with anterior displacement of C1. C1-laminectomy improved the progressive paresis. Progressive paresis caused by spinal cord compression is a hitherto unrecognized complication in patients with CDG-Ia.
引用
收藏
页码:115 / 117
页数:3
相关论文
共 50 条
  • [11] A mouse model for congenital disorder of glycosylation IA
    Schneider, A.
    Thiel, C.
    Rindermann, J.
    Koerner, C.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2007, 30 : 66 - 66
  • [12] Biochemical and molecular analysis of a patient with congenital disorder of glycosylation type Ia.
    Wood, TC
    Flannery, D
    Kottra, J
    Longshore, J
    Taylor, H
    AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 488 - 488
  • [13] Conotruncal heart defects in three patients with congenital disorder of glycosylation type IA
    Romano, S.
    Valayannopoulos, V.
    Lyonnet, S.
    Seta, N.
    Bonnet, D.
    Sidi, D.
    de Lonlay, P.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2007, 30 : 65 - 65
  • [14] Risk assessment of acute vascular events in congenital disorder of glycosylation type Ia
    Arnoux, J. B.
    Boddaert, N.
    Valayannopoulos, V.
    Romano, S.
    Bahi-Buisson, N.
    Desguerre, I.
    de Keyzer, Y.
    Munnich, A.
    Brunelle, F.
    Seta, N.
    Dautzenberg, M. D.
    de Lonlay, P.
    MOLECULAR GENETICS AND METABOLISM, 2008, 93 (04) : 444 - 449
  • [15] Risk assessment of acute vascular events in congenital disorder of glycosylation type IA
    Arnoux, J. B.
    Valayannopoulos, V.
    Boddaert, N.
    Desguerre, I
    Brunelle, F.
    Seta, N.
    Dautzenberg, M. D.
    de Lonlay, P.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2007, 30 : 64 - 64
  • [16] A mouse model for congenital disorder of glycosylation IA (CDG-IA)
    Schneider, A.
    Thiel, C.
    Groene, H. J.
    Koerner, C.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2008, 31 : 49 - 49
  • [17] Leukocyte phosphomannomutase activity and congenital disorder of glycosylation Ia
    Barnier, A
    Dupré, T
    Cuer, M
    Vuillaumier-Barrot, S
    Durand, G
    Seta, N
    GLYCOBIOLOGY, 2001, 11 (10) : 905 - 905
  • [18] Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology
    Aronica, E
    van Kempen, AAMW
    van der Heide, M
    Poll-The, BT
    van Slooten, HJ
    Troost, D
    Rozemuller-Kwakkel, JM
    ACTA NEUROPATHOLOGICA, 2005, 109 (04) : 433 - 442
  • [19] Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology
    E. Aronica
    A. A. M. W. van Kempen
    M. van der Heide
    B. T. Poll-The
    H. J. van Slooten
    D. Troost
    J. M. Rozemuller-Kwakkel
    Acta Neuropathologica, 2005, 109 : 433 - 442
  • [20] Congenital disorder of glycosylation type Ia: benign clinical course in a new genetic variant
    Irina Mader
    Marion Döbler-Neumann
    Wilhelm Küker
    Helena Stibler
    Ingeborg Krägeloh-Mann
    Child's Nervous System, 2002, 18 : 77 - 80