Chiari in the Family: Inheritance of the Chiari I Malformation

Pediatric Neurology

Volumn 34, Issue 6, 2006, Pages 481-485

  Szewka, Aimee J ^a   Walsh, Laurence E ^a   Boaz, Joel C ^a   Carvalho, Karen S ^a   Golomb, Meredith R ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHIARI FROMMEL SYNDROME; CHILDHOOD; CLINICAL FEATURE; HEADACHE; HUMAN; LITERATURE; MALE; MONOZYGOTIC TWINS; PATHOGENESIS; PRESCHOOL CHILD; PRIORITY JOURNAL; RIGIDITY; SIBLING; SWALLOWING; SYMPTOM; SYMPTOMATOLOGY; SYRINGOMYELIA;

ADULT; ARNOLD-CHIARI MALFORMATION; CHILD; DISEASES IN TWINS; FEMALE; HUMANS; INFANT; INHERITANCE PATTERNS; MALE; PEDIGREE; TWINS, MONOZYGOTIC;

EID: 33744931100     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2005.09.008     Document Type: Article

References (30)

1. Ford F.R. Diseases of the nervous system in infancy, childhood, and adolescence. Chapter 1: Prenatal diseases and developmental defects of the nervous system (1973), Charles C. Thomas, Springfield, IL 100-102
2. Atkinson J.L., Kokmen E., and Miller G.M. Evidence of posterior fossa hypoplasia in the familial variant of adult Chiari I malformation. Case report. Neurosurgery 42 (1998) 401-403
3. Cavender R., and Schmidt J. Tonsillar ectopia and Chiari malformation. Monozygotic triplets. J Neurosurg 82 (1995) 497-500
4. Coria F., Quintana F., Rebollo M., Combarros O., and Berciano J. Occipital dysplasia and Chiari type I deformity in a family. Clinical and radiological study of three generations. J Neurol Sci 62 1-3 (1983) 147-158
5. George S., and Page A. Familial Chiari 1 malformation. The Eye, 2005 (2005) 1-3. http://www.nature.com/eye Advance online publication. www.nature.com/eye, 22 Apr
6. Gripp K.W., Scott Jr. C.I., Nicholson L., Magram G., and Grissom L.E. Chiari malformation and tonsillar ectopia in twin brothers and father with autosomal dominant spondylo-epiphyseal dysplasia tarda. Skeletal Radiol 26 (1997) 131-133
7. Herman M.D., Cheek W.R., Storrs B.B., et al. Two siblings with the Chiari I malformation. Pediatr Neurosurg 16 (1990) 183-184
8. Mavinkurve G.G., Sciubba D., Amundson E., and Jallo G.I. Familial Chiari type I malformation with syringomyelia in two siblings. Case report and review of the literature. Childs Nerv System (2005). http://www.springerlink.com Advance online publication, www.springerlink.com, April 9, 2005.
9. Milhorat T.H., Chou M.W., Trinidad E.M., et al. Chiari I malformation redefined. Clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 44 (1999) 1005-1017
10. Speer M.C., George T.M., Enterline D.S., Franklin A., Wolpert C., and Milhorat T.H. A genetic hypothesis for Chiari I malformation with or without syringomyelia. Neurosurg Focus 8 (2000) 1-4
11. Stovner L.J. Headache and Chiari type I malformation. Occurrence in female monozygotic twins and first-degree relatives. Cephalalgia 12 (1992) 304-307
12. Stovner L.J., and Sjaastad O. Segmental hyperhidrosis in two siblings with Chiari type I malformation. Eur Neurol 35 (1995) 149-155
13. Tubbs R.S., Wellons 3rd J.C., Blount J.P., and Oakes W.J. Syringomyelia in twin brothers discordant for Chiari I malformation. Case report. J Child Neurol 19 (2004) 459-462
14. Zakeri A., Glasauer F.E., and Egnatchik J.G. Familial syringomyelia. Case report and review of the literature. Surg Neurol 44 (1995) 48-53
15. Stovner L.J., Cappelen J., Nilsen G., and Sjaastad O. The Chiari type I malformation in two monozygotic twins and first-degree relatives. Ann Neurol 31 (1992) 220-222
16. Colombo A., and Cislaghi M.G. Familial syringomyelia. Case report and review of the literature. Ital J Neurol Sci 14 (1993) 637-639
17. Yabe I., Kikuchi S., and Tashiro K. Familial syringomyelia. The first Japanese case and review of the literature. Clin Neurol Neurosurg 105 (2002) 69-71
18. Rusbridge C., and Knowler S.P. Inheritance of occipital bone hypoplasia (Chiari type I malformation) in Cavalier King Charles spaniels. J Veterinary Intern Med 18 (2004) 673-678
19. Nishikawa M., Sakamoto H., Hakuba A., Nakanishi N., and Inoue Y. Pathogenesis of Chiari malformation. A morphometric study of the posterior cranial fossa. J Neurosurg 86 (1997) 40-47
20. Schijman E. History, anatomic forms, and pathogenesis of Chiari I malformations. Childs Nerv System 20 (2004) 323-328
21. Gardner W. Hydrodynamic mechanism of syringomyelia. Its relationship to myelocele. J Neurol Neurosurg Psychiatry 28 (1965) 247-259
22. Levine D.N. The pathogenesis of syringomyelia associated with lesions at the foramen magnum. A critical review of existing theories and proposal of a new hypothesis. [see comment]. J Neurol Sci 220 1-2 (2004) 3-21
23. Dyste G.N., and Menezes A.H. Presentation and management of pediatric Chiari malformations without myelodysplasia. Neurosurgery 23 (1988) 589-597
24. Steinbok P. Clinical features of Chiari I malformations. Childs Nerv System 20 (2004) 329-331
25. Brill C.B., Gutierrez J., and Mishkin M.M. Chiari Type 1 malformation. Association with seizures and developmental disabilities. J Child Neurol 12 (1997) 101-106
26. Brockmeyer D., Gollogly S., and Smith J.T. Scoliosis associated with Chiari 1 malformations: The effect of suboccipital decompression on scoliosis curve progression: A preliminary study. Spine 28 (2003) 2505-2509
27. Eule J.M., Erickson M.A., O'Brien M.F., and Handler M. Chiari I malformation associated with syringomyelia and scoliosis. A twenty-year review of surgical and nonsurgical treatment in a pediatric population. Spine 27 (2002) 1451-1455
28. Inoue M., Nakata Y., Minami S., et al. Idiopathic scoliosis as a presenting sign of familial neurologic abnormalities. Spine 28 (2003) 40-45
29. Ono A., Ueyama K., Okada A., Echigoya N., Yokoyama T., and Harata S. Adult scoliosis in syringomyelia associated with Chiari I malformation. Spine 27 (2002) 23-28
30. Sponseller P.D. Syringomyelia and Chiari I malformation presenting with juvenile scoliosis as sole manifestation. J Spinal Disord 5 (1992) 237-239