Arthrogryposis multiplex congenita in a child with congenital fractures: a case report

被引:0
|
作者
Kavinda Dayasiri
Heshan Jayaweera
机构
[1] University of Kelaniya,Department of Paediatrics, Faculty of Medicine
[2] University of Peradeniya,Department of Paediatrics
来源
Journal of Medical Case Reports | / 16卷
关键词
Arthrogryposis; Bruck syndrome; Case report;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [31] Arthrogryposis multiplex congenita: Perinatal and electromyographic findings, disability, and psychosocial outcome
    Sodergard, J
    HakamiesBlomqvist, L
    Sainio, K
    Ryoppy, S
    Vuorinen, R
    JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B, 1997, 6 (03): : 167 - 171
  • [32] Feasibility and Challenges of Performing Magnetoencephalography Experiments in Children With Arthrogryposis Multiplex Congenita
    Golosheykin, Semyon A.
    Blagoveschenskiy, Evgueni D.
    Agranovich, Olga E.
    Nazarova, Maria A.
    Nikulin, Vadim V.
    Moiseenko, Olesya E.
    Chan, Russell W.
    Shestakova, Anna N.
    FRONTIERS IN PEDIATRICS, 2021, 9
  • [33] Development of an online registry for adults with arthrogryposis multiplex congenita: A protocol paper
    Sawatzky, Bonita
    Dahan-Oliel, N.
    Davison, Ann-Marie
    Hall, Judith
    Van Bosse, Harold
    Ben Mortenson, W.
    Yadav, S.
    Mortenson, B.
    Noonan, V
    Schalk, T.
    Sidebottom, N.
    Nouraei, H.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2019, 181 (03) : 454 - 460
  • [34] Validation of the Oswestry Disability Index for pain and disability in arthrogryposis multiplex congenita
    Jones, Talon
    Miller, Rebecca
    Street, John T.
    Sawatzky, Bonita
    ANNALS OF PHYSICAL AND REHABILITATION MEDICINE, 2019, 62 (02) : 92 - 97
  • [35] Osteogenesis imperfecta with arthrogryposis multiplex congenita (Bruck syndrome) - evidence for possible autosomal recessive inheritance
    Brady, AF
    Patton, MA
    CLINICAL DYSMORPHOLOGY, 1997, 6 (04) : 329 - 336
  • [36] ARTHROGRYPOSIS MULTIPLEX IN A NEWBORN OF A MYASTHENIC MOTHER - CASE-REPORT AND LITERATURE
    DINGER, J
    PRAGER, B
    NEUROMUSCULAR DISORDERS, 1993, 3 (04) : 335 - 339
  • [37] Arthrogryposis multiplex congenita: Etiology, genetics, classification, diagnostic approach, and general aspects
    Hall, JG
    JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B, 1997, 6 (03): : 159 - 166
  • [38] Arthrogryposis multiplex congenita: Blood vessel hypoplasia and implications during renal transplantation
    Soon, S
    Kapoor, A
    Ludwin, D
    Russell, D
    Whelan, P
    JOURNAL OF UROLOGY, 2001, 165 (01) : 174 - 174
  • [39] Arthrogryposis multiplex congenita: Functional classification and the AMC disc-o-gram
    Mennen, U
    JOURNAL OF HAND SURGERY-BRITISH AND EUROPEAN VOLUME, 2004, 29B (04) : 363 - 367
  • [40] Arthrogryposis multiplex congenita and bilateral parietal polymicrogyria in association with the in intrauterine death of a twin
    Baker, EM
    Khouasgani, MG
    GardnerMedwin, D
    Gholkar, A
    Griffiths, PD
    NEUROPEDIATRICS, 1996, 27 (01) : 54 - 56