Siblings of Schwartz-Jampel Syndrome with abnormal muscle computed tomographic findings

被引:3
作者
Iwata, H
Ozawa, H
Kamei, A
Sasaki, M
Hanaoka, S
Sugai, K
Hashimoto, T
Nonaka, I
机构
[1] Natl Ctr Neurol & Psychiat, Natl Ctr Hosp Mental Nervous & Muscular Disorders, Tokyo 1878551, Japan
[2] Iwate Med Univ, Dept Pediat, Morioka, Iwate, Japan
关键词
Schwartz-Jampel syndrome; sibling cases; abnormal muscle computed tomography findings;
D O I
10.1016/S0387-7604(00)00184-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Schwartz-Jampel syndrome (SJS) is a disorder characterized by myotonia, joint contractures. skeletal abnormalities, facial dysmorphism and growth retardation. We present two boys of ages 4 and 8 years with SJS. Their clinical, electromyographic and histopathological findings were similar to those described, except fur computed tomography (CT) images that revealed diffuse high attenuation in sternocleidomastoid muscles and low attenuation in the paraspinal, quadriceps. sartorius, soleus and gastrocunemius muscles. This is the first report describing abnormal muscle CT findings associated with SJS. Additional studies of muscle CT might help to improve understanding of the pathogenesis of SJS. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:494 / 497
页数:4
相关论文
共 9 条
  • [1] BUICKE JA, 1979, NEURORADIOLOGY, V17, P127
  • [2] SCHWARTZ-JAMPEL SYNDROME - CLINICAL, ELECTROPHYSIOLOGICAL AND HISTOPATHOLOGICAL STUDY OF A SEVERE VARIANT
    CAO, A
    CIANCHETTI, C
    CALISTI, L
    DEVIRGILIIS, S
    FERRELI, A
    TANGHERONI, W
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1978, 35 (2-3) : 175 - 187
  • [3] SCHWARTZ-JAMPEL SYNDROME - AN ATYPICAL FORM
    FIGUERA, LE
    JIMENEZGIL, FJ
    GARCIACRUZ, MO
    CANTU, JM
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (04): : 526 - 528
  • [4] Recessive Schwartz-Jampel syndrome (SJS']JS): Confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS']JS locus to a 3-cM interval
    Fontaine, B
    Nicole, S
    Topaloglu, H
    BenHamida, C
    Beighton, P
    Spaans, F
    Cantu, JMA
    Bakouri, S
    Romero, N
    Ricker, K
    BarrosNunez, P
    Ponsot, G
    BenHamida, M
    Weissenbach, J
    Hentati, F
    LehmannHorn, F
    [J]. HUMAN GENETICS, 1996, 98 (03) : 380 - 385
  • [5] FOWLER WM, 1974, J NEUROL SCI, V22, P127
  • [6] CHONDRODYSTROPHIC MYOTONIA (SCHWARTZ-JAMPEL SYNDROME) IN SOUTH-AFRICAN CHILDREN
    MOODLEY, M
    MOOSA, A
    [J]. NEUROPEDIATRICS, 1990, 21 (04) : 206 - 210
  • [7] NONAKA I, 1992, SKELETAL MUSCLE PATH, P337
  • [8] IMPROVEMENT OF MYOTONIA WITH CARBAMAZEPINE IN 3 CASES WITH SCHWARTZ-JAMPEL SYNDROME
    TOPALOGLU, H
    SERDAROGLU, A
    OKAN, M
    GUCUYENER, K
    TOPCU, M
    [J]. NEUROPEDIATRICS, 1993, 24 (04) : 232 - 234
  • [9] VISSER M, 1994, MYOLOGY, P795