Adenovirus serotype 31 infection in a newborn girl and review of the literature

Abstract

References1 Sanyanusin P, Schimmenti LA, McNoe LA et al. Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. Nat. Genet. 1995; 9: 358-64. 2 Cheong HI, Cho HY, Kim JH, Yu YS, Ha IS, Choi Y. A clinicogenetic study of renal coloboma syndrome in children. Pediatr. Nephrol. 2007; 22: 1283-9. 3 Amiel J, Audollent S, Joly D et al. PAX2 mutations in renalcoloboma syndrome: Mutational hotspot and germline mosaicism. Eur. J. Hum. Genet. 2000; 8: 820-6. 4 Ford B, Rupps R, Lirenman D et al. Renal-coloboma syndrome: Prenatal detection and clinical spectrum in a large family. Am. J. Med. Genet. 2001; 99: 137-41. 5 Martinovic-Bouriel J, Benachi A, Bonniere M et al. PAX2 mutations in fetal renal hypodysplasia. Am. J. Med. Genet. A 2010; 152A: 830-5. 6 Curry CJ, 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. 7 Nishimoto K, Iijima K, Shirakawa T et al. PAX2 gene mutation in a family with isolated renal hypoplasia.