Öz
Dandy-Walker variant is a rare anomaly of the central nervous system that is characterized by partial agenesis of vermis and results in persistence of the 4. ventricule and cisterna magna. Firstly, in 1988 Kohyama et al. [10] reported the coexistence of Dandy-Walker variant and tetralogy of Fallot. Afterwards, it is reported as several case reports in the literature. In this case report, we report a 2 days-old male patient with Dandy-Walker variant and pentalogy of Fallot.
Anahtar Kelimeler
Kaynakça
- Millen KJ, Gleeson JG. Disorders of Cerebellar and Brainstem Development. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, eds. Swaiman’s Pediatric neurology: principles and practice. 5th ed. Philadelphia: Elsevier Saunders 2012; 160Barkovich AJ. Congenital Malformations of the Brain and Skull. Pediatric Neuroimaging. 4th ed. Philadelphia: Lippincott Williams&Wilkins 2005; 387-91. Tadakamadla J, Kumar S, Mamatha GP. Dandy-Walker malformation: An incidental finding. Indian J Hum Genet 2010; 16: 33-5.
- Ozdemir O, Polat A, Cinbis M, Kurt F, Kucuktasci K, Kiroglu Y. DandyWalker's variant and tetralogy of Fallot with atrial septal defect and patent ductus arteriosus and primary hypothyroidy--a new association. Indian J Pediatr 2009; 76: 433-5.
- Sasaki-Adams D, Elbabaa SK, Jewells V, Carter L, Campbell JW, Ritter AM. The Dandy-Walker variant: A case series of 24 pediatric patients and evaluation of associated anomalies, incidence of hydrocephalus, and developmental outcomes. J Neurosurg Pediatr 2008; 2: 194-9.
- Poetke M, Frommeld T, Berlien HP. PHACE syndrome: new views on diagnostic criteria. Eur J Pediatr Surg 2002; 12: 366-74.
- Leonardi ML, Pai GS, Wilkes B, Lebel RR. Ritscher-Schinzel cranio-cerebellocardiac (3C) syndrome: report of four new cases and review. Am J Med Genet 2001; 102: 237-42.
- Hsieh CC, Hsu JJ, Lo LM, Hsieh TT, Soong YK. Non-mosaic trisomy 20 in cultures of amniotic fluid from a fetus with serious congenitale malformation. J Formos Med Assoc 1992; 91: 543-4.
- Hirsch JF, Kahn AP, Renier D, Rose CS, Hirsch EH. The Dandy-Walker malformation. J Neurosurg 1984; 61: 515-22.
- Kohyama J, Watanabe S, Iwakawa Y, Fukuda C. A case of Dandy-Walker malformation: consideration on the teratogenic period and sleep structures. Brain Dev 1988; 10: 392-6.
Öz
Özet
Dandy-Walker varyasyonu, 4. ventrikül ve sisterna magna arasındaki devamlılıkla sonuçlanan vermisin parsiyel agenezisi ile karakterize santral sinir sisteminin nadir bir anomalisidir. Literatürde ilk kez 1988’de Kohyama ve arkadaşları tarafından bildirilen Dandy-Walker varyasyonu ve Fallot Tetralojisi birlikteliği daha sonraki yıllarda birkaç vaka sunumu şeklinde bildirilmiştir. Biz bu yazıda, Dandy-Walker varyasyonu ve Fallot Pentalojisi olan 2 günlük bir erkek hastayı bildiriyoruz.
Anahtar sözcükler: Dandy-Walker varyasyonu, Fallot Pentalojisi
Abstract
Dandy-Walker variant is a rare anomaly of the central nervous system that is characterized by partial agenesis of vermis and results in persistence of the 4. ventricule and cisterna magna. Firstly, in 1988 Kohyama et al. reported the coexistence of Dandy-Walker variant and tetralogy of Fallot. Afterwards, it is reported as several case reports in the literature. In this case report, we report a 2 days-old male patient with Dandy-Walker variant and pentalogy of Fallot.
Keywords: Dandy-Walker variant, pentalogy of Fallot
Anahtar Kelimeler
Kaynakça
- Millen KJ, Gleeson JG. Disorders of Cerebellar and Brainstem Development. In: Swaiman KF, Ashwal S, Ferriero DM, Schor NF, eds. Swaiman’s Pediatric neurology: principles and practice. 5th ed. Philadelphia: Elsevier Saunders 2012; 160Barkovich AJ. Congenital Malformations of the Brain and Skull. Pediatric Neuroimaging. 4th ed. Philadelphia: Lippincott Williams&Wilkins 2005; 387-91. Tadakamadla J, Kumar S, Mamatha GP. Dandy-Walker malformation: An incidental finding. Indian J Hum Genet 2010; 16: 33-5.
- Ozdemir O, Polat A, Cinbis M, Kurt F, Kucuktasci K, Kiroglu Y. DandyWalker's variant and tetralogy of Fallot with atrial septal defect and patent ductus arteriosus and primary hypothyroidy--a new association. Indian J Pediatr 2009; 76: 433-5.
- Sasaki-Adams D, Elbabaa SK, Jewells V, Carter L, Campbell JW, Ritter AM. The Dandy-Walker variant: A case series of 24 pediatric patients and evaluation of associated anomalies, incidence of hydrocephalus, and developmental outcomes. J Neurosurg Pediatr 2008; 2: 194-9.
- Poetke M, Frommeld T, Berlien HP. PHACE syndrome: new views on diagnostic criteria. Eur J Pediatr Surg 2002; 12: 366-74.
- Leonardi ML, Pai GS, Wilkes B, Lebel RR. Ritscher-Schinzel cranio-cerebellocardiac (3C) syndrome: report of four new cases and review. Am J Med Genet 2001; 102: 237-42.
- Hsieh CC, Hsu JJ, Lo LM, Hsieh TT, Soong YK. Non-mosaic trisomy 20 in cultures of amniotic fluid from a fetus with serious congenitale malformation. J Formos Med Assoc 1992; 91: 543-4.
- Hirsch JF, Kahn AP, Renier D, Rose CS, Hirsch EH. The Dandy-Walker malformation. J Neurosurg 1984; 61: 515-22.
- Kohyama J, Watanabe S, Iwakawa Y, Fukuda C. A case of Dandy-Walker malformation: consideration on the teratogenic period and sleep structures. Brain Dev 1988; 10: 392-6.
Ayrıntılar
| Birincil Dil | Türkçe |
|---|---|
| Bölüm | Olgu Sunumları |
| Yazarlar | |
| Yayımlanma Tarihi | 9 Haziran 2014 |
| Yayımlandığı Sayı | Yıl 2014Cilt: 36 Sayı: 3 |