Agenesis of the Corpus Callosum: a Rare Association with Ehlers-Danlos Syndrome
Iranian Journal of Child Neurology,
Vol. 14 No. 4 (2020),
1 October 2020
,
Page 95-99
https://doi.org/10.22037/ijcn.v14i4.21232
Abstract
Ehlers-Danlos syndrome (EDS) is a rare congenital disorder of connective tissues which involves the skin and musculoskeletal system. There are also some reports for the involvement of the central and peripheral nervous systems. We want to present a very rare coassociation of EDS, spondylolisthesis, and Agenesis of the corpus callosum in an Iranian lady.
- Ehlers-Danlos syndrome
- spondylolisthesis
- Agenesis of the corpus callosum
How to Cite
References
Ansari G, FallahinejadGhajari M, Nazemi B, Erfanian B. Dental Considerations in Ehlers-Danlos Syndrome: A Case Report. J ComprPed. 2015 ;6(1):e22463.
Sheen VL, Jansen A, Chen MH, Parrini E, Morgan T, Ravenscroft R, et al. Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome. Neurology. 2005;64(2):254–62.
Dotti MT, de Stefano N, Mondillo S, Agricola E, Federico A. Neurological involvement and quadricuspid aortic valve in a patient with 4.Ehlers-Danlos syndrome. J Neurol. 1999;246(7):612–3.
Echaniz-Laguna A, de Saint-Martin A, Lafontaine AL, Tasch E, Thomas P, Hirsh E, et al. Bilateral focal polymicrogyria in Ehlers-Danlos syndrome. Arch Neurol. 2000;57(1):123–7.
Hagino H, Eda I, Takashima S, Takeshita K, Sugitani A. Computed tomography in patients with Ehlers-Danlos syndrome. Neuroradiology. 1985;27(5):443–5.
Brunk I, Stover B, Ikonomidou C, Brinckmann J, Neumann LM. Ehlers-Danlos syndrome type VI with cystic malformations of the meninges in a 7-year-old girl. Eur J Pediatr. 2004;163(4-5):214–7.
J.acome DE. Headache in Ehlers-Danlos syndrome. Cephalalgia. 1999;19(9):791–6
Castori M, Camerota F, Celletti C, Danese C, Santilli V, SaraceniVM, et al. Natural history and manifestations of the hypermobility type Ehlers-Danlos syndrome: a pilot study on 21 patients. Am J Med Genet A. 2010;152A(3):556–64.
Pretorius ME, Butler IJ. Neurologic manifestations of Ehlers-Danlos syndrome. Neurology. 1983;33(8):1087–9.
Galan E, Kousseff BG. Peripheral neuropathy in Ehlers-Danlos syndrome. Pediatr Neurol. 1995;12(3):242–5.
Gomez-Garre P, Seijo M, Gutierrez-Delicado E, Castro del RM, de la Torre C, Gomez-Abad C, et al. Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation. J Med Genet. 2006;43(3):232–7.
Rombaut L, Malfait F, Cools A, De Paepe A, Calders P. Musculoskeletal complaints, physical activity and health-related quality of life among patients with the Ehlers-Danlos syndrome hypermobility type. DisabilRehabil. 2010;32(16):1339–45
Davidovitch M, Tirosh E, Tal Y. The relationship between joint hypermobility and neurodevelopmental attributes in elementary school children. J Child Neurol. 1994;9(4):417–9.
Castori M, Morlino S, Celletti C, Ghibellini G, Bruschini M, Grammatico P, et al. Re-writing the natural history of pain and related symptoms in the joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type. Am J Med Genet A. 2013;161A(12):2989–3004
Marco Castori1 and Nicol C. Voermans. Neurological manifestations of Ehlers-Danlos syndrome(s): A review; Iran J Neurol. 2014 Oct 6; 13(4): 190–208.
- Abstract Viewed: 275 times