Urinary retention in a boy with terminal deletion of chromosome 10q at band 26.1
2008; Wiley; Volume: 50; Issue: 4 Linguagem: Inglês
10.1111/j.1442-200x.2008.02683.x
ISSN1442-200X
AutoresOsamu Motoyama, Mika Tokuyama, Naoki Uga, Kikuo Iitaka,
Tópico(s)Urological Disorders and Treatments
ResumoPediatrics InternationalVolume 50, Issue 4 p. 603-604 Urinary retention in a boy with terminal deletion of chromosome 10q at band 26.1 Osamu Motoyama, Corresponding Author Osamu Motoyama 1Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Chiba, Departments of 2Pediatrics and 3Neonatology, Toho University Medical Center, Omori Hospital, Tokyo and 4Department of Pediatrics, Yamato City Hospital, Kanagawa, JapanOsamu Motoyama, MD, Department of Pediatrics, Toho University Medical Center, Sakura Hospital, 564-1 Shimoshizu, Sakura-shi, Chiba 285-8741, Japan. Email: [email protected]Search for more papers by this author 1 Mika Tokuyama, Mika Tokuyama 1Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Chiba, Departments of 2Pediatrics and 3Neonatology, Toho University Medical Center, Omori Hospital, Tokyo and 4Department of Pediatrics, Yamato City Hospital, Kanagawa, JapanSearch for more papers by this author 2 Naoki Uga, Naoki Uga 1Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Chiba, Departments of 2Pediatrics and 3Neonatology, Toho University Medical Center, Omori Hospital, Tokyo and 4Department of Pediatrics, Yamato City Hospital, Kanagawa, JapanSearch for more papers by this author 3 Kikuo Iitaka, Kikuo Iitaka 1Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Chiba, Departments of 2Pediatrics and 3Neonatology, Toho University Medical Center, Omori Hospital, Tokyo and 4Department of Pediatrics, Yamato City Hospital, Kanagawa, JapanSearch for more papers by this author 4 Osamu Motoyama, Corresponding Author Osamu Motoyama 1Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Chiba, Departments of 2Pediatrics and 3Neonatology, Toho University Medical Center, Omori Hospital, Tokyo and 4Department of Pediatrics, Yamato City Hospital, Kanagawa, JapanOsamu Motoyama, MD, Department of Pediatrics, Toho University Medical Center, Sakura Hospital, 564-1 Shimoshizu, Sakura-shi, Chiba 285-8741, Japan. Email: [email protected]Search for more papers by this author 1 Mika Tokuyama, Mika Tokuyama 1Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Chiba, Departments of 2Pediatrics and 3Neonatology, Toho University Medical Center, Omori Hospital, Tokyo and 4Department of Pediatrics, Yamato City Hospital, Kanagawa, JapanSearch for more papers by this author 2 Naoki Uga, Naoki Uga 1Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Chiba, Departments of 2Pediatrics and 3Neonatology, Toho University Medical Center, Omori Hospital, Tokyo and 4Department of Pediatrics, Yamato City Hospital, Kanagawa, JapanSearch for more papers by this author 3 Kikuo Iitaka, Kikuo Iitaka 1Department of Pediatrics, Toho University Medical Center, Sakura Hospital, Chiba, Departments of 2Pediatrics and 3Neonatology, Toho University Medical Center, Omori Hospital, Tokyo and 4Department of Pediatrics, Yamato City Hospital, Kanagawa, JapanSearch for more papers by this author 4 First published: 25 August 2008 https://doi.org/10.1111/j.1442-200X.2008.02683.xCitations: 2Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article. References 1 Leonard NJ, Harley FL, Lin CC. Terminal deletion of chromosome 10q at band 26.1: Follow-up in an adolescent male with high-output renal failure from congenital obstructive uropathy. Am. J. Med. Genet. 1999; 86: 115– 17. 2 Ogata T, Muroya K, Sasagawa I et al. Genetic evidence for a novel gene(s) involved in urogenital development on 10q26. Kidney Int. 2000; 58: 2281– 90. 3 Gorinati M, Zamboni G, Padoin N, Dodero A, Caufin D, Memo L. Terminal deletion of long arm of chromosome 10: Case report and review of the literature. Am. J. Med. Genet. 1989; 33: 502– 4. 4 International Reflux Study Committee. Medical versus surgical treatment of primary vesicoureteral reflux: A prospective international reflux study in children. J. Urol. 1981; 125: 277– 83. 5 Kogasaka R, Morohoshi T, Sawada Y, Fujiwara M. Terminal deletion of chromosome 10q and its clinical features. Acta Paediatr. Jpn. 1990; 32: 83– 7. 6 Bauer SB. Neuropathology of the lower urinary tract. In: PP Kelalis, LR King, AB Belman (eds). Clinical Pediatric Urology, 3rd edn. WB Saunders, Philadelphia, 1992; 399– 440. 7 Wright FS. Disorders of micturition and defecation. In: KF Swaiman, FS Wright (eds). The Practice of Pediatric Neurology, 2nd edn. CV Mosby, St Louis, 1982; 318– 26. 8 Shapiro SD, Hansen KL, Pasztor LM et al. Deletions of the long arm of chromosome 10. Am. J. Med. Genet. 1985; 20: 181– 96. Citing Literature Volume50, Issue4August 2008Pages 603-604 ReferencesRelatedInformation
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