Öz
Congenital bilateral perisylvian syndrome (CBPS), which is seen by indications of mental retardasyon, epilepsi, speech disorder and pseudobulbar palsy, is a disease which comes up with genetic and non-genetic reasons. Revealing characteristic indications (like polymicrogyria) with MR imaging and clinic indications contributes making diagnosis. In present paper, we aimed to present 18 month girl case report who diagnosed as CBPS with hydrocephali indication.
Anahtar Kelimeler
Epilepsy congenital bilateral perisylvian syndrome polymicrogyria hydrocephalus pseudobulbar palsy
Kaynakça
- Naidich T.P., Kang E., Fatterpekar G.M. et al. The insula: anatomic study and MR imaging display at 1.5 T. Am J Neuroradiol 2004;25 (2):222-32.
- Gropman AL, Barkovich AJ, Vezina LG, Conry JA, Dubovsky EC, Packer RJ. Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients. Neuropediatrics 1997; 28(1): 198-203.
- Kuzniecky R, Andermann F, Guerrini R. Congenital bilateral perisylvian syndrome: study of 31 patients.The CBPS Multicenter Collaborative Study. Lancet 1993; 341(4): 608-612.
- Harding, BCA. Malformations. In: Graham, DILP, editor. Greenfield’s Neuropathology. 6th Ed. London: Arnold; 1997. p. 387-533.
- Barkovich AJ,Hevnera R,GuerriniaR. Syndromes of bilateral symmetrical polymicrogyria AJNR Am J Neuroradiol 1999;19(20): 1814-21.
- Barkovich AJ, Lindan CE. Congenital cytomegalovirus infection of the brain: imaging analysis and embryologic considerations AJNR Am J Neuroradiol 1994;15(4):703-15.
- Tamaoki Y,Kishi K, Yamaguchi S. A variant case of congenital bilateral perisylvian syndrome with asymmetric findings on neuroimaging and septum pellucidum defect. Brain Dev 2001;23(1):131-4.
Öz
Konjenital bilateral slyvian sendrom (KBPS) mental retardasyon, epilepsi, konuşma bozukluğu, psödobulbar palsi gibi bulgularla kendini gösteren, genetik ve genetik dışı nedenlerle ortaya çıkan konjenital bir hastalıktır. Klinik bulgularla birlikte, MR görüntüleme ile karakteristik bulguların (polimikrogiri gibi) ortaya konması, tanı konulmasında katkı sağlamaktadır. Yazımızda hidrosefali bulgusu bulunan KBPS tanısı konulan 18 aylık kız çocuğu olgusunu sunmayı amaçladık.
Anahtar Kelimeler
Epilepsi konjenital perisilvian sendrom polimikrogri hidrosefali psödobulbar palsi
Kaynakça
- Naidich T.P., Kang E., Fatterpekar G.M. et al. The insula: anatomic study and MR imaging display at 1.5 T. Am J Neuroradiol 2004;25 (2):222-32.
- Gropman AL, Barkovich AJ, Vezina LG, Conry JA, Dubovsky EC, Packer RJ. Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients. Neuropediatrics 1997; 28(1): 198-203.
- Kuzniecky R, Andermann F, Guerrini R. Congenital bilateral perisylvian syndrome: study of 31 patients.The CBPS Multicenter Collaborative Study. Lancet 1993; 341(4): 608-612.
- Harding, BCA. Malformations. In: Graham, DILP, editor. Greenfield’s Neuropathology. 6th Ed. London: Arnold; 1997. p. 387-533.
- Barkovich AJ,Hevnera R,GuerriniaR. Syndromes of bilateral symmetrical polymicrogyria AJNR Am J Neuroradiol 1999;19(20): 1814-21.
- Barkovich AJ, Lindan CE. Congenital cytomegalovirus infection of the brain: imaging analysis and embryologic considerations AJNR Am J Neuroradiol 1994;15(4):703-15.
- Tamaoki Y,Kishi K, Yamaguchi S. A variant case of congenital bilateral perisylvian syndrome with asymmetric findings on neuroimaging and septum pellucidum defect. Brain Dev 2001;23(1):131-4.
Ayrıntılar
| Birincil Dil | Türkçe |
|---|---|
| Bölüm | Olgu Sunumu |
| Yazarlar | |
| Yayımlanma Tarihi | 1 Aralık 2012 |
| Yayımlandığı Sayı | Yıl 2012 Cilt: 3 Sayı: 4 |