Cervical disc prolapse in childhood associated with Klippel-Feil syndrome

被引:8
|
作者
Allsopp, GM
Griffiths, S
Sgouros, S
机构
[1] Birmingham Childrens Hosp, Inst Child Hlth, Birmingham B4 6NH, W Midlands, England
[2] Birmingham Childrens Hosp, Dept Neurosurg, Birmingham B4 6NH, W Midlands, England
关键词
Klippel-Feil syndrome; cervical spine; discectomy;
D O I
10.1007/s003810000377
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Klippel-Feil syndrome is characterized by a variable degree of congenital fusion of the cervical spine. It can exist in association with other mesodermal deformities affecting several systems. Symptomatic cervical disc prolapse in the context of the syndrome is well documented in young adults. We present a case of a 5-year-old girl with the syndrome, who presented with mild motor developmental delay and cervical cord compression from a prolapsed C3/4 intervertebral disc, seen on MR scan. She also had posterior elements fused from C-2 to C-4. She improved after cervical discectomy. The presence of degenerative disc disease at such a young age and at a level mechanically protected by posterior element fusion indicates a congenital primary defect, rather than mechanical stress fatigue.
引用
收藏
页码:69 / 70
页数:2
相关论文
共 50 条
  • [41] Clinical Approach to Patients with Klippel-Feil Syndrome
    Kaya, Murat
    Kabaklioglu, Murat
    Eroz, Recep
    KONURALP TIP DERGISI, 2021, 13 (01): : 135 - 140
  • [42] Otolaryngologic Manifestations of Klippel-Feil Syndrome in Children
    Kenna, Margaret A.
    Irace, Alexandria L.
    Strychowsky, Julie E.
    Kawai, Kosuke
    Barrett, Devon
    Manganella, Juliana
    Cunningham, Michael J.
    JAMA OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2018, 144 (03) : 238 - 243
  • [43] Cervical canal stenosis caused by progressive fusion and enlargement of cervical vertebrae with features of Proteus syndrome and Klippel-Feil syndrome
    Sugita, Shurei
    Chikuda, Hirotaka
    Ohya, Junichi
    Taniguchi, Yuki
    Takeshita, Katsushi
    Haga, Nobuhiko
    Ushiku, Tetsuo
    Tanaka, Sakae
    SKELETAL RADIOLOGY, 2013, 42 (12) : 1743 - 1746
  • [44] Klippel-Feil Syndrome: Pathogenesis, Diagnosis, and Management
    Litrenta, Jody
    Bi, Andrew S.
    Dryer, Joseph W.
    JOURNAL OF THE AMERICAN ACADEMY OF ORTHOPAEDIC SURGEONS, 2021, 29 (22) : 951 - 960
  • [45] Heterogeneity in Klippel-Feil syndrome: a new classification
    Clarke, RA
    Catalan, G
    Diwan, AD
    Kearsley, JH
    PEDIATRIC RADIOLOGY, 1998, 28 (12) : 967 - 974
  • [46] KLIPPEL-FEIL SYNDROME, A SKELETAL MUSCLE DISEASE ASSOCIATED TO CARDIOVASCULAR ANOMALIES
    de Rubens-Figueroa, Jesus
    Zepeda-Orozco, Gabriela
    Gonzalez-Rosas, Alma
    BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO, 2005, 62 (05): : 348 - 355
  • [47] Klippel-Feil Syndrome (KFS) with Multiple Cervical Anomalies Discovered Following Trauma
    Celi, Fernando
    Saal-Zapata, Giancarlo
    INDIAN JOURNAL OF NEUROTRAUMA, 2021, 18 (01): : 69 - 71
  • [48] Mutations in PAX1 may be associated with Klippel-Feil syndrome
    McGaughran, JM
    Oates, A
    Donnai, D
    Read, AP
    Tassabehji, M
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2003, 11 (06) : 468 - 474
  • [49] KLIPPEL-FEIL SYNDROME AND DANDY-WALKER MALFORMATION
    Karaman, A.
    Kahveci, H.
    GENETIC COUNSELING, 2011, 22 (04): : 411 - 415
  • [50] Cochlear Implant in Klippel-Feil Syndrome: Challenges and Concerns
    Reddy, Y. Mounika
    Lepcha, Anjali
    Augustine, Ann Mary
    Philip, Ajay
    INDIAN JOURNAL OF OTOLARYNGOLOGY AND HEAD & NECK SURGERY, 2022, 74 (SUPPL 3) : 3901 - 3905