Www.formudes.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorders/Hemih dwb.unl.edu/Teacher/NSF/C11/C11Links/www.sleeptight.com/EncyMaster/H/hemihypertrophy.html NodeWorks Genetic Disorders hemihypertrophy other. thumbnail, 1. DrHull - An article about hemihypertrophy,what it is, the features, follow up and prognosis. thumbnail, 2 http://www.formudes.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorder
Health Conditions And Diseases Genetic Disorders Hemihypertrophy Health Conditions and Diseases Genetic Disorders hemihypertrophy Directoryresults Some web results for Genetic Disorders hemihypertrophy http://world.ammissione.it/browse_/Health/Conditions_and_Diseases/Genetic_Disord
Wuup.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorders/Hemihypertrop www.phatnav.com/directory/Health/Conditions_and_Diseases/Genetic_Disorders/hemihypertrophy.cat www.sweden.org/Health/Conditions_and_Diseases/Genetic_Disorders/hemihypertrophy/ Guests of the Hemi Web Site Visitor chris ceraso Reference hemihypertrophy website Location Sewell, nj WebSiteWeb Info Contact chrismagcer@comcast.net Date Fri, Apr 23, 2004 at 15 http://wuup.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorders/Hemihy
NWTSG Patient Information Page children with Wilms tumor registered in a national clinical trial during 196981showed high rates of aniridia, hemihypertrophy, cryptorchidism, hypospadias http://www.nwtsg.org/public/patient_info.html
Extractions: Publications of Interest: Breslow NE, Beckwith JB: Epidemiological features of Wilms' tumor: results of the National Wilms' Tumor Study. Journal of the National Cancer Institute 68(3): 429-436, 1982. Nearly 2,000 children with Wilms' tumor registered in a national clinical trial during 1969-81 showed high rates of aniridia, hemihypertrophy, cryptorchidism, hypospadias, and other genitourinary anomalies. Patients with bilateral disease, who constituted 5% of the total, had younger ages at diagnosis and an increased incidence of congenital anomalies and renal blastemal rests. Those with multicentric unilateral lesions had more blastemal rests but were otherwise indistinguishable from the unicentric cases. The 20 familial cases had none of the features usually associated with genetic tumors: neither younger ages nor an increase in bilaterality nor associated congenital anomalies. These observations suggest that the fraction of Wilms' tumors that is due to an inherited mutation may be substantially smaller than previously supposed and support the concept that the disease arises from a variety of pathogenetic pathways. (Author abstract) (38 Refs)
