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
  • [1] Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type IA
    Coman, D.
    Bostock, D.
    Hunter, M.
    Kannu, P.
    Irving, M.
    Mayne, V
    Fietz, M.
    Jaeken, J.
    Savarirayan, R.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2007, 30 : 65 - 65
  • [2] Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type Ia
    Coman, D.
    Bostock, D.
    Hunter, M.
    Kannu, P.
    Irving, M.
    Mayne, V.
    Fietz, M.
    Jaeken, J.
    Savarilrayan, R.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (03) : 389 - 392
  • [3] Assessment of skeletal status in patients with congenital disorder of glycosylation type IA
    Barone, R
    Pavone, V
    Pennisi, P
    Fiumara, A
    Fiore, CE
    INTERNATIONAL JOURNAL OF TISSUE REACTIONS-EXPERIMENTAL AND CLINICAL ASPECTS, 2002, 24 (01): : 23 - 28
  • [4] Macular Hypoplasia in Congenital Disorder of Glycosylation Type Ia
    Wang, Bob Z.
    Siriwardana, Pradeep
    Taranath, Deepa
    CASE REPORTS IN OPHTHALMOLOGY, 2012, 3 (01): : 142 - 144
  • [5] Congenital disorder of glycosylation type Ia presenting with hydrops fetalis
    van de Kamp, J. M.
    Lefeber, D. J.
    Ruijter, G. J. G.
    Steggerda, S. J.
    den Hollander, N. S.
    Willems, S. M.
    Matthijs, G.
    Poorthuis, B. J. H. M.
    Wevers, R. A.
    JOURNAL OF MEDICAL GENETICS, 2007, 44 (04) : 277 - 280
  • [6] THROMBOPHILIA IN CONGENITAL DISORDER OF GLYCOSYLATION TYPE IA - A CASE STUDY
    Azevedo, A.
    Pereira, J.
    Gomes, A.
    Reis, A.
    Junior, E.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2010, 95 : 765 - 765
  • [7] Stabilization of hypoglycosylation in a patient with congenital disorder of glycosylation type Ia
    Hahn, SH
    Minnich, SJ
    O'Brien, JF
    JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 (01) : 235 - 237
  • [8] Pericardial and abdominal fluid accumulation in Congenital Disorder of Glycosylation type Ia
    Truin, Gerben
    Guillard, Mailys
    Lefeber, Dirkj.
    Sykut-Cegielska, Jolanta
    Adarnowicz, Madej
    Hoppenreijs, Esther
    Sengers, Rob C. A.
    Wevers, Ron A.
    Morava, Eva
    MOLECULAR GENETICS AND METABOLISM, 2008, 94 (04) : 481 - 484
  • [9] A MOUSE MODEL FOR CONGENITAL DISORDER OF GLYCOSYLATION IA
    Thiel, C.
    Rindermann, J.
    Luebke, T.
    Matthijs, G.
    Von Figura, K.
    Koerner, C.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 : 199 - 199
  • [10] Conotruncal heart defects in three patients with congenital disorder of glycosylation type Ia (CDG Ia)
    Romano, S.
    Bajolle, F.
    Valayannopoulos, V.
    Lyonnet, S.
    Colomb, V.
    de Barace, C.
    Vouhe, P.
    Pouard, P.
    Vuillaumier-Barrot, S.
    Dupre, T.
    de Keyzer, Y.
    Sidi, D.
    Seta, N.
    Bonnet, D.
    de Lonlay, P.
    JOURNAL OF MEDICAL GENETICS, 2009, 46 (04) : 287 - 288