Chiari I Malformations and the Heritable Disorders of Connective Tissue

被引:4
作者
Ellington, Meghan [1 ]
Francomano, Clair A. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Med & Mol Genet, 975 W Walnut St,IB 130, Indianapolis, IN 46202 USA
关键词
Chiari I malformation; Heritable disorders of connective tissue; Ehlers-Danlos syndrome; Marfan syndrome; Complex Chiari; EHLERS-DANLOS-SYNDROME; MARFAN-SYNDROME; HYPERMOBILITY; MANIFESTATIONS; HERNIATION; HEADACHE; PATIENT;
D O I
10.1016/j.nec.2022.09.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
[No abstract available]
引用
收藏
页码:61 / 65
页数:5
相关论文
共 29 条
  • [1] Hemifacial spasm in a patient with Marfan syndrome and Chiari I malformation
    Braca, J
    Hornyak, M
    Murali, R
    [J]. JOURNAL OF NEUROSURGERY, 2005, 103 (03) : 552 - 554
  • [2] The complex Chiari: issues and management strategies
    Brockmeyer, Douglas L.
    [J]. NEUROLOGICAL SCIENCES, 2011, 32 : 345 - 347
  • [3] Natural History and Manifestations of the Hypermobility Type Ehlers-Danlos Syndrome: A Pilot Study on 21 Patients
    Castori, Marco
    Camerota, Filippo
    Celletti, Claudia
    Danese, Chiara
    Santilli, Valter
    Saraceni, Vincenzo Maria
    Grammatico, Paola
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (03) : 556 - 564
  • [4] Resolution of cervical syringomyelia after transoral odontoidectomy and occipitocervical fusion in a patient with basilar invagination and Type I Chiari malformation
    Dickman, Curtis A.
    Yashar, M.
    Kalani, S.
    [J]. JOURNAL OF CLINICAL NEUROSCIENCE, 2012, 19 (12) : 1726 - 1728
  • [5] MARFAN-SYNDROME CAUSED BY A RECURRENT DENOVO MISSENSE MUTATION IN THE FIBRILLIN GENE
    DIETZ, HC
    CUTTING, GR
    PYERITZ, RE
    MASLEN, CL
    SAKAI, LY
    CORSON, GM
    PUFFENBERGER, EG
    HAMOSH, A
    NANTHAKUMAR, EJ
    CURRISTIN, SM
    STETTEN, G
    MEYERS, DA
    FRANCOMANO, CA
    [J]. NATURE, 1991, 352 (6333) : 337 - 339
  • [6] Ehlers Danlos Society The, DIAGNOSTIC CRITERIA
  • [7] Greally MT, 1998, AM J MED GENET, V76, P202, DOI 10.1002/(SICI)1096-8628(19980319)76:3<202::AID-AJMG2>3.0.CO
  • [8] 2-S
  • [9] Greally MT, 2006, GENEREVIEWS
  • [10] Cervical medullary syndrome secondary to craniocervical instability and ventral brainstem compression in hereditary hypermobility connective tissue disorders: 5-year follow-up after craniocervical reduction, fusion, and stabilization
    Henderson, Fraser C., Sr.
    Francomano, C. A.
    Kohy, M.
    Tuchman, K.
    Adcock, J.
    Patel, S.
    [J]. NEUROSURGICAL REVIEW, 2019, 42 (04) : 915 - 936