Fetal akinesia sequence caused by nemaline myopathy

被引:45
作者
Lammens, M
Moerman, P
Fryns, JP
Lemmens, F
vandeKamp, GM
Goemans, N
Dom, R
机构
[1] UNIV HOSP GASTHUISBERG,DEPT NEUROPATHOL,B-3000 LOUVAIN,BELGIUM
[2] UNIV HOSP GASTHUISBERG,DEPT PATHOL 1,B-3000 LOUVAIN,BELGIUM
[3] UNIV HOSP GASTHUISBERG,DEPT PEDIAT,B-3000 LOUVAIN,BELGIUM
[4] UNIV HOSP GASTHUISBERG,CTR HUMAN GENET,B-3000 LOUVAIN,BELGIUM
[5] ST JANSZIEKENHUIS,DEPT PEDIAT,GENK,BELGIUM
[6] ST JOSEPHZIEKENHUIS,NEONATAL INTENS CARE UNIT,VELDHOVEN,NETHERLANDS
关键词
nemaline myopathy; fetal akinesia sequence; arthrogryposis multiplex congenita; Pena Shokeir syndrome;
D O I
10.1055/s-2007-973683
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Nine patients with the characteristic signs of fetal akinesia sequence (polyhydramnion, multiple joint contractures and lung hypoplasia) are described. in 8 of the 9 patients nemaline myopathy could be demonstrated with histology., The ninth patient presented the same phenotype as his 4 affected siblings in whom the nemaline myopathy could be histologically proven. Seven of the patients belonged to 2 families; the other 2 patients were isolated cases. in one fetal case nemaline myopathy was documented at week 22 of gestation. These observations demonstrate that nemaline myopathy can cause the fetal akinesia sequence, with onset of first symptoms as early as the beginning of the second trimester of pregnancy.
引用
收藏
页码:116 / 119
页数:4
相关论文
共 20 条
  • [1] ARTHROGRYPOSIS MULTIPLEX CONGENITA - SPECTRUM OF PATHOLOGICAL-CHANGES
    BANKER, BQ
    [J]. HUMAN PATHOLOGY, 1986, 17 (07) : 656 - 672
  • [2] NEONATAL NEMALINE MYOPATHY WITH ABUNDANT INTRANUCLEAR RODS
    BAROHN, RJ
    JACKSON, CE
    KAGANHALLET, KS
    [J]. NEUROMUSCULAR DISORDERS, 1994, 4 (5-6) : 513 - 520
  • [3] NEONATAL NEMALINE MYOPATHY PRESENTING WITH MULTIPLE JOINT CONTRACTURES
    BUCHER, HU
    BOLTSHAUSER, E
    BRINER, J
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1985, 144 (03) : 288 - 290
  • [4] DUBOWITZ V, 1985, MUSCLE BIOPSY MODERN
  • [5] THE PATHOGENESIS OF FETAL HYPOKINESIA - A NEUROLOGICAL STUDY OF 75 CASES OF CONGENITAL CONTRACTURES WITH EMPHASIS ON CEREBRAL-LESIONS
    HAGEMAN, G
    WILLEMSE, J
    VANKETEL, BA
    VERDONCK, AFMM
    [J]. NEUROPEDIATRICS, 1987, 18 (01) : 22 - 33
  • [6] CONGENITAL NEMALINE MYOPATHY WITH DILATED CARDIOMYOPATHY - AN AUTOPSY STUDY
    ISHIBASHIUEDA, H
    IMAKITA, M
    YUTANI, C
    TAKAHASHI, S
    YAZAWA, K
    KAMIYA, T
    NONAKA, I
    [J]. HUMAN PATHOLOGY, 1990, 21 (01) : 77 - 82
  • [7] A MUTATION IN THE ALPHA-TROPOMYOSIN GENE TPM3 ASSOCIATED WITH AUTOSOMAL-DOMINANT NEMALINE MYOPATHY
    LAING, NG
    WILTON, SD
    AKKARI, PA
    DOROSZ, S
    BOUNDY, K
    KNEEBONE, C
    BLUMBERGS, P
    WHITE, S
    WATKINS, H
    LOVE, DR
    HAAN, E
    [J]. NATURE GENETICS, 1995, 9 (01) : 75 - 79
  • [8] FATAL NEONATAL NEMALINE MYOPATHY WITH MULTIPLE CONGENITAL ANOMALIES
    MCCOMB, RD
    MARKESBERY, WR
    OCONNOR, WN
    [J]. JOURNAL OF PEDIATRICS, 1979, 94 (01) : 47 - 51
  • [9] MIDDLETON LT, 1995, NEUROMUSCULAR DISORD, V4, P273
  • [10] MOERMAN P, 1908, VIRCHOWS ARCH A, V410, P339