VACTERL BİRLİKTELİĞİ VE POTTER SEKANSI

Öz

     

Anahtar Kelimeler

• VACTERL birlikteliği, potter sekansı, yenidoğan

Kaynakça

1. Curry CJR, Jensen K, Holland J, Miller L, Hall BD. The Potter sequence: A clinical analysis of 80 cases. Am J Med Genet 1984;19: 679-702.
2. Keckler SJ, St.Peter SD, Valusek PA, Tsao K, Snyder CL, Holcomb III GW, Ostlie DJ.VACTERL anomalies in patients with esophageal atresia: An updated delineation of the spectrum and review of the literature. Pediatr Surg Int 2007; 23: 309-313.
3. Kolon TF, Gray CL, Sutherland, RW, Roth DR, Gonzales ET Jr. Upper urinary tract manifestations of the VACTERL association. J Urol 2000; 163: 1949-1951.
4. Lukusa T, Moerman P, Fryns JP. Caudal developmental field defect with female pseudohermaphroditism and VACTERL anomalies. Genet Couns 1996; 7: 207-212.
5. Martinez-Frias ML, Frias JL . Primary developmental field III: Clinical and epidemioogical study of blastogenetic anomalies and their relationship to different MCA patterns. Am J Med Genet 1997;70: 11-15.
6. Opitz JM. Blastogenesis and the “Primary Field ‟‟ in Human Development. In: Alan R. Liss, Inc., for the National Foundation-March of Dimes. BD:OAS XXIX (1): 3-37, New York 1993.
7. Quan L, Smith DW. The VATER association. Vertebral defects, anal atresia, T-E fistula with esophageal atresia, radial and renal dysplasia: A spectrum of associated defects. J Pediatr 1973; 82: 104-107.
8. Uehling DT, Gilbert E, Chesney R. Urologic implications of the VATER association. J Urol 1983;129: 352-354.

9. Ahn SY, Mendoza S, Kaplan G, Reznik V. Chronic kidney disease in the VACTERL association: clinical course and outcome. Pediatr Nephrol 2009; 24: 1047-1053.