Club Feet with Congenital Perisylvian Polymicrogyria Possibly Due to Bifocal Ischemic Damage of the Neuraxis in Utero

American Journal of Medical Genetics

Volumn 126 A, Issue 2, 2004, Pages 191-196

  Kammoun, Fatma ^a,e   Tanguy, Alain ^b   Boesplug Tanguy, Odile ^b   Bensahel, Henri ^c   Khouri, Nejib ^d   Landrieu, Pierre ^a  

^a BICÊTRE HOSPITAL   (France)

^b UNIVERSITY HOSPITAL OF CLERMONT FERRAND   (France)

^c BICHAT HOSPITAL   (France)

^d SAINT JOSEPH HOSPITAL   (France)

^e HABIB BOURGUIBA HOSPITAL   (Tunisia)

Author keywords

Club foot; Perisylvian cortical dysplasia; Pierre Marie Foix Chavany syndrome; Vascular compromise

Indexed keywords

ARTICLE; BRAIN ISCHEMIA; CASE REPORT; CLUBFOOT; DYSARTHRIA; ELECTROPHYSIOLOGY; EPILEPSY; FAMILY STUDY; FEMALE; GENE REARRANGEMENT; GENETIC ANALYSIS; GESTATIONAL AGE; HUMAN; INTESTINE ATRESIA; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; MICROGYRIA; NERVE FIBER; NERVE INJURY; NEUROPATHY; NEWBORN; PERISYLVIAN POLYMICROGYRIA; PRIORITY JOURNAL; SPINAL CORD LESION;

EID: 1842533446     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20562     Document Type: Article

References (33)

1. Banker BQ. 1986. Arthrogryposis multiplex congenita: Spectrum of pathological changes. Hum Pathol 17:656-672.
2. Becker PS, Dixon AM, Truncoso JC. 1989. Bilateral opercular polymicrogyria. Ann Neurol 25:90-92.
3. Bingham PM, Lynch D, McDonald-McGinn D, Zackai E. 1998. Polymicrogyria in chromosome 22 deletion syndrome. Neurology 51:1500-1502.
4. Bleck EE. 1993. Club foot. Dev Med Child Neurol 35:927-931.
5. Bordarier C, Robain O, Ponsot G. 1991. Bilateral porencephalic defect in a newborn after injection of benzol during pregnancy. Brain Dev 13: 126-129.
6. Brodtkorb E, Torbergsen T, Nakken KO, Andersen K, Gimse R, Sjaastad O. 1994. Epileptic seizures, arthrogryposis, and migrational brain disorders: A syndrome? Acta Neurol Scand 90:232-240.
7. Clark M, Carr L, Reilly S, Neville B. 2000. Worster-Drought syndrome, a mild tetraplegic perisylvian cerebral palsy: Review of 47 cases. Brain 123:2160-2170.
8. Dekaban A. 1965. Large defects in cerebral hemisphere associated with cortical dysgenesis. J Neuropath Exp Neurol 24:512-530.
9. Fedrizzi E, Botteon G, Inverno M, Ciceri E, D'Incerti L, Dworzak F. 1993. Neurogenic arthrogryposis multiplex congenita: Clinical and MRI findings. Pediatr Neurol 9:343-348.
10. Fukuhara K, Schollmeier G, Uhthoff HK. 1994. The pathogenesis of club foot. A histomorphemetric and immunohistochemical study of fetuses. J Bone Joint Surg Br 76:450-457.
11. Gray DH, Katz JM. 1981. A histochemical study of muscle in club foot. J Bone Joint Surg Br 63-B:417-423.
12. Gropman AL, Barkovich AJ, Vezina LG, Conry JA, Dubovsky EC, Packer RJ. 1997. Pediatric congenital bilateral perisylvian syndrome: Clinical and MRI features in 12 patients. Neuropediatrics 28:198-203.
13. Guerreiro MM, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K, Van Bogaert P, Gillain C, David P, Ambrosetto G, Rosati A, Bartolomei F, Parmeggiani A, Paetau R, Salonen O, Ignatius J, Borgatti R, Zucca C, Bastos AC, Palmini A, Fernandes W, Montenegro MA, Cendes F, Andermann F. 2000. Familial perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment. Ann Neurol 48: 39-48.
14. Hageman G, Hoogenraad TU, Prevo RL. 1994. The association of cortical dysplasia and anterior horn arthrogryposis: A case report. Brain Dev 16:463-466.
15. Hevner RF, Horoupian DS. 1996. Pena-Shokeir phenotype associated with bilateral opercular polymicrogyria. Pediatr Neurol 15:348-351.
16. Humbertclaude V, Pedespan JM, Azais M, Fontan D, Echenne B. 1996. Schizencephaly and upper limb malformation. Arch Pediatr 3:357-359.
17. Ippolito E. 1995. Update on pathologic anatomy of clubfoot. J Pediatr Orthop B 4:17-24.
18. Kawashima T, Uhthoff HK. 1990. Development of the foot in prenatal life in relation to idiopathic club foot. J Pediatr Orthop 10:232-237.
19. Kimber CP, MacMahon RA, Shekleton P, Yardley R. 1997. Antenatal intestinal vascular accident with subsequent small bowel atresia: Case report. Ultrasound Obstet Gynecol 10:212-214.
20. Kuker W, Friese S, Riethmuller J, Krageloh-Mann I. 2000. Congenital bilateral perisylvian syndrome (CBPS): Do concomitant oesophageal malformations indicate a poor prognosis? Neuropediatrics 31:310-313.
21. Kuzniecky R, Andermann F, Guerrini R. 1993. Congenital bilateral perisylvian syndrome: Study of 31 patients. The CBPS Multicenter Collaborative Study. Lancet 341(8845):608-612.
22. Levine DN, Fisher MA, Caviness V. 1974. Porencephaly with microgyria, a pathological study. Acta Neuropathol 29:99-113.
23. Lochmiller C, Johnston D, Scott A, Risman M, Hecht JT. 1998. Genetic epidemiology study of idiopathic talipes equinovarus. Am J Med Genet 79:90-96.
24. Macnicol MF, Nadeem RD. 2000. Evaluation of the deformity in club foot by somatosensory evoked potentials. J Bone Joint Surg 82:731-735.
25. Marques-Dias MY, Harmant-Van Rijckevorsel G, Landrieu P, Lyon G. 1989. Prenatal cytomegalovirus disease and cerebral microgyria: Evidence for perfusion failure, not disturbance of histogenesis, as the major cause of foetal cytomegalovirus encephalopathy. Acta Neuropathol 99: 26-37.
26. Nadeem RD, Brown JK, Lawson G, Macnicol MF. 2000. Somatosensory evoked potentials as a means of assessing neurological abnormality in congenital talipes equinovarus. Dev Med Child Neurol 42:525-530.
27. Reid CO, Hall JG, Anderson C, Bocian M, Carey J, Costa T, Curry C, Greenberg F, Horton W, Jones M, Lafer C, Larson E, Lubinsky M, McGillivray B, Pembry M, Popkin J, Seller M, Siebert V, Verhagen A. 1986. Association of amyoplasia with gastroschisis, bowel atresia, and defects of the muscular layer of the trunk. Am J Med Genet 24:701-710.
28. Robertson WL, Glinski LP, Kirkpatrick SJ, Pauli RM, 1992. Further evidence that arthrogryposis multiplex congenita in the human sometimes is caused by an intrauterine vascular accident. Teratology 45:345-351.
29. Rousseau S, Metral S, Lacroix C, Cahusac C, Nocton F, Landrieu P. 1993. Anterior spinal artery syndrome mimicking infantile spinal muscular atrophy. Am J Perinatol 10:316-318.
30. Sébire G, Husson B, Navelet Y, Tardieu M, Dusser A, Landrieu P. 1996. Unilateral congenital perisylvian syndrome. Radiological basis and clinical correlations. J Neurol Neurosurg Psychiat 61:52-56.
31. Van Bogaert P, David P, Gillain CA, Wikler D, Damhaut P, Scalais E, Nuttin C, Wetzburger C, Szliwowski HB, Metens T, Goldman S. 1998. Perisylvian dysgenesis. Clinical, EEG, MRI and glucose metabolism features in 10 patients. Brain 121:2229-2238.
32. Villard L, Nguyen K, Cardoso C, Martin CL, Weiss AM, Sifry-Platt M, Grix AW, Graham JM, Jr., Winter RM, Leventer RJ, Dobyns WB. 2002. A locus for bilateral perisylvian polymicrogyria maps to Xq28. Am J Hum Genet 70:1003-1008.
33. Ward PJ, Clarke NM, Fairhurst JJ. 1998. The role of magnetic resonance imaging in the investigation of spinal dysraphism in the child with lower limb abnormality. J Pediatr Orthop 7:141-143.