41. Health Conditions And Diseases C Gambling@ 75 Congenital Arthromyodysplasia@ 98 Congenital Facial Diplegia@5 Congenital Heart Disease@ 46 congenital nephroblastoma@ 4 Congenital http://www.pastconnect.com/odp/directory/Health/Conditions_and_Diseases/C/

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42. Health Conditions And Diseases C Diplegia @ (5); Congenital Heart Disease @ (46); congenital nephroblastoma@ (4); Congenital Pain Insensitivity @ (2); Conjunctivitis http://freshlinks.net/odp.aspx/Health/Conditions_and_Diseases/C/

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43. Katalog :  : Health : Conditions_and_Diseases : C :  - Netz-Tipp.De Heart Disease (*); congenital nephroblastoma (*); Congenital PainInsensitivity (*); Conjunctivitis (*); Constipation (*); Continuous http://www.netz-tipp.de/kat/Health/Conditions_and_Diseases/C/

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44. Health > Conditions And Diseases > C Congenital Heart Disease; congenital nephroblastoma; Congenital PainInsensitivity; Conjunctivitis; Constipation. Continuous Muscle Fiber http://www.xasa.com/directorio/mozilla/Top/Health/Conditions_and_Diseases/C/

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45. GREENSEEK congenital nephroblastoma@ (4); Congenital Pain Insensitivity@ (2); Genetic Disorders@(630). See also Health Conditions and Diseases Congenital Anomalies (3). http://www.greenseek.de/internet/index.php/Health/Child_Health/Conditions_and_Di

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46. HealthCentral - General Encyclopedia - Wilms Tumor Alternative names tumor Wilms; kidney tumor; nephroblastoma It is associated withcertain congenital defects including urinary tract abnormalities, absence http://www.healthcentral.com/mhc/top/001575.cfm

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47. Entrez PubMed ultrastructure; nephroblastoma/congenital*; nephroblastoma/genetics; nephroblastoma/ultrastructure.PMID 3030229 PubMed indexed for MEDLINE http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?holding=npg&cmd=Retrieve&db=PubMed

48. Entrez PubMed pathology*; Kidney Neoplasms/ultrastructure; Male; Microscopy, Electron/methods;Nephrectomy; nephroblastoma/congenital; nephroblastoma http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?holding=npg&cmd=Retrieve&db=PubMed

49. Mesoblastic Nephroma The group of tumors with a better prognosis encompasses congenital mesoblasticnephroma (CMN), fetal rhabdomyomatous nephroblastoma and cystic, partially http://www.thedoctorsdoctor.com/diseases/kidney_mesoblastic_nephroma.htm

Background This is a rare, usually congenital, neoplasm of the kidney. It was first identified in the kidneys sent in for Wilm's tumors and indeed the chief differential diagnosis is with this latter malignant tumor of the kidney. OUTLINE Epidemiology Disease Associations Pathogenesis Laboratory/Radiologic/Other Diagnostic Testing ... Internet Links EPIDEMIOLOGY CHARACTERIZATION INCIDENCE Rare AGE RANGE-MEDIAN Usually congenital DISEASE ASSOCIATIONS CHARACTERIZATION HYPERCALCEMIA Hypercalcemia in association with mesoblastic nephroma: report of a case and review of the literature. Ferraro EM, Klein SA, Fakhry J, Weingarten MJ, Rose JS. Pediatr Radiol 1986;16(6):516-7 Abstract quote Hypercalcemia, often associated with certain types of adult tumors, has also been described in pediatric neoplasms. In childhood, the more common associations include lymphoma, leukemia, rhabdomyosarcoma and rarely neuroblastoma. However, recently, several infants with hypercalcemia were described having renal tumors without bone metastases. The following is a case report of a 2-month-old infant who presented with severe hypercalcemia and a large right-sided abdominal mass, which at surgery was diagnosed as a cellular mesoblastic nephroma.

50. Kidney Image URL congenital renal dysplasia, Image URL congenital renal dysplasia,Image URL Diabetes, Image URL nephroblastoma, Image URL nephroblastoma, http://www.brisbio.ac.uk/ROADS/subject-listing/kidney.html

A collection of medical, dental and veterinary images for use in teaching. Home About the Archive FAQ Terms and Conditions ... Help Kidney Accelerated glomerulonephritis Acute diffuse proliferative glomerulonephritis Acute diffuse proliferative glomerulonephritis Acute diffuse proliferative glomerulonephritis Acute diffuse proliferative glomerulonephritis Acute interstitial nephritis Acute interstitial nephritis Acute interstitial nephritis Acute interstitial nephritis Acute proliferative glomerulonephritis Acute proliferative glomerulonephritis Acute pyelitis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute pyelonephritis Acute renal failure Acute renal failure Acute renal failure Acute renal failure Acute renal failure Acute renal failure Acute renal failure Acute renal failure Acute renal failure Acute tubular necrosis Acute, exudative proliferative glomerulonephritis

51. Results Of The Search congenital Wilms tumors are mostly (benign) mesoblastic nephromassignificanceof prenatally detected nephroblastoma and Wilms tumor in hemihypertrophy. http://invention.swmed.edu/trite/abstracts/user-1016145454/results.shtml

New This Month New This Year Submitted paragraph Wilms' tumour as a paradigm for the relationship of cancer to development. K Pritchard-Jones ... N D Hastie Cancer Surv 1990 ;9(3);555-78. Score: 0.83 Molecular genetics of Wilms' tumour. J S Tay J Paediatr Child Health 1995 Oct;31(5);379-83. Score: 0.78 [Anaplastic type of Wilms' tumour] G M Vujani? ... S Aleksandrovi? Srp Arh Celok Lek 1990 Sep-Oct;118(9-10);353-6. Score: 0.74 Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. P Grundy ... W K Cavenee Nature 1988 Nov;336(6197);374-6. Score: 0.74 Teratoid Wilms' tumour: a report of two cases. J F Magee ... J Dimmick Histopathology 1992 May;20(5);427-31. Score: 0.73 Molecular and cellular biology of Wilms' tumour. N J Maitland ... J Williams Anticancer Res 1989 Sep-Oct;9(5);1417-26. Score: 0.73 Cell types expressing the Wilms' tumour gene (WT1) in Wilms' tumours: implications for tumour histogenesis. K Pritchard-Jones ... S Fleming Oncogene 1991 Dec;6(12);2211-20. Score: 0.73 Role of the WT1 gene in Wilms' tumour. D A Haber ... D E Housman Score: 0.72

52. TheFetus.net - Congenital Mesoblastic Nephroma -Andreas Rempen, MD,Thomas Kirchn Sonography cannot provide a clear distinction between congenital mesoblasticnephroma and nephroblastoma (Wilms tumor) because both are essentially http://www.thefetus.net/page.php?id=508

53. TheFetus.net - Neuroblastoma -Angela Regina Capelanes, MD*, Gloria Valero, MD&, Prenatal diagnosis of congenital Wilms tumor (nephroblastoma) presenting asfetal hydrops. Ultrasound in Obstetrics and Gynecology 16 (1), 8083l. http://www.thefetus.net/page.php?id=521

54. Sorry - Www.biomedcentral.com Is Temporarily Unavailable Human; Hypertrophy; Karyotyping; nephroblastoma/complications*; nephroblastoma/congenital.Substances Gonadotropins. PMID 4294698 PubMed http://www.biomedcentral.com/pubmed/4294698

Sorry - www.biomedcentral.com is temporarily unavailable due to maintenance. Please contact info@biomedcentral.com if the problem persists. Note that all research articles published by BioMed Central are available for download from our mirrors, such as PubMed Central BioMed Central authors (and potential authors): Apologies for the inconvenience. Please come back soon to submit your manuscript.

55. Anterior Abdominal Wall - DIAGNOSIS OF CONGENITAL ABNORMALITIES - THE 18-23 WEEK hypoglycemia. About 5% of affected individuals develop tumors during childhood,most commonly nephroblastoma and hepatoblastoma. Prevalence. http://www.centrus.com.br/DiplomaFMF/SeriesFMF/18-23-weeks/chapter-06/abdome_fmf

Anterior Abdominal Walll Handbook of Fetal Abnormalities Algorithms Appendix Anterior abdominal wall Normal Sonography Anatomy Exomphalos Gastroschisis Body Stalk Anomaly ... Authors NORMAL SONOGRAPHIC ANATOMY Normal development of the anterior abdominal wall depends on the fusion of four ectomesodermic folds (cephalic, caudal and two lateral). At 8–10 weeks of gestation, all fetuses demonstrate herniation of the mid-gut that is visualized as a hyperechogenic mass in the base of the umbilical cord; retraction into the abdominal cavity occurs at 10–12 weeks and is completed by 11 weeks and 5 days. The integrity of the abdominal wall should always be demonstrated; this can be achieved by transverse scans demonstrating the insertion of the umbilical cord. It is also important to visualize the urinary bladder within the fetal pelvis, because this rules out exstrophy of the bladder and of the cloaca. EXOMPHALOS Exomphalos results from failure of normal embryonic regression of the mid-gut from the umbilical stalk into the abdominal celom. The abdominal contents, including intestines and liver or spleen covered by a sac of parietal peritoneum and amnion, are herniated into the base of the umbilical cord.

56. ORPHANET - Rare Diseases - Orphan Drugs nephroblastoma or Wilms tumor is the most frequent renal tumor in children nephroblastomasmay be associated with a variety of congenital malformations (aniridia http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=654

57. ORPHANET® : Nephroblastoma Summary nephroblastoma or Wilms tumor is the most frequent renal tumor in nephroblastomasmay be associated with a variety of congenital malformations (aniridia http://www.orpha.net/static/GB/nephroblastoma.html

Orphanet database access Nephroblastoma Direct access to data Summary Update : 01/06/2004 Orphanet database access

58. Cancer Syndromes WAGR) syndrome; Wilms tumor associated with congenital absence of Additional featuresWilms tumor (nephroblastoma), gonadoblastoma, hemangioma, and pigmented http://ibis-birthdefects.org/start/cancersy.htm

Tips for printing Cancer Syndromes About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Please Explore: Support Groups Professional Associations Key Information Sources Topics include Title and Nephroblastoma Aniridia,Type II Wims Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Wilms Tumor 3 Wilms Tumor 2 Multiple Tumor Associated Chromosome Region 1 Special Resources Cancer Syndrome A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Groups Online Mendelian Inheritance in Man by OMIM ANIRIDIA ... ANIRIDIA, CEREBELLAR ATAXIA ... WAGR SYNDROME ... ANIRIDIA AND ABSENT PATELLA ... WILMS TUMOR 1 ... ECTOPIA PUPILLAE ... CAT EYE SYNDROME ... PETERS ANOMALY ... EXOSTOSES ... SPLIT-HAND/FOOT ... Wilms Tumor Nephroblastoma by OMIM Rather numerous instances of multiple sibs with Wilms tumor have been described ... The syndrome of aniridia, hemihypertrophy and other congenital anomalies with Wilms tumor, subsequently known as the WAGR syndrome, was first described by Miller et al. (1964) ... . Riccardi et al. (1978) observed a triad of aniridia, ambiguous genitalia and mental retardation (AGR triad) in 3 patients with an interstitial deletion of the short arm of chromosome 11 ... Marshall et al. (1982) studied 14 patients with aniridia .... 6 had interstitial deletion of 11p of various lengths. Band 11p13 was included in the deletion in all 6 cases ...

59. Www.whonamedit.com syndrome). A congenital syndrome in which aniridia and nephroblastoma(Wilms tumour) is associated with multiple abnormalities. Aniridia http://www.whonamedit.com/syndlist.cfm/193

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Eponyms in category: Multiple congenital anomalies 188 main and alternative entries found. Aase-Smith syndrome A familial deformity syndrome. Aase’s syndrome (Aase-Smith syndrome) A familial deformity syndrome. Alè-Calò syndrome (Langer-Giedion syndrome) Syndrome characterized by a combination of mental retardation and a long list of physical abnormalities, including multiple extoses, peculiar facies, and loose redundant skin. Alfi's syndrome A very rare chromosome anomaly also known as monosomy 9P. Aniridia-Wilms' tumor association (Brusa-Torricelli syndrome) A congenital syndrome in which aniridia and nephroblastoma (Wilms' tumour) is associated with multiple abnormalities.

60. Brusa-Torricelli Syndrome (www.whonamedit.com) BrusaTorricelli syndrome A congenital syndrome in which aniridia and nephroblastoma(Wilms tumour) is associated with multiple abnormalities. http://www.whonamedit.com/synd.cfm/2404.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Brusa-Torricelli syndrome Also known as: Aniridia-Wilms’ tumour syndrome Aniridia-Wilms' tumor association Miller’s syndrome (R. W. Miller) Synonyms: Aniridia-nephroblastoma syndrome, oculocerebrorenal syndrome. Associated persons: P. Brusa R. W. Miller C. Torricelli Max Wilms Description: A congenital syndrome in which aniridia (congenital absence of the iris) and nephroblastoma (Wilms' tumour) is associated with mental retardation, craniofacial defects (microcephaly), growth retardation and skeletal anomalies, deformed pinna, genitourinary anomalies, hamartomas, and umbilical and inguinal hernias. Other frequent features include cataract and glycoma, hypospadias, hemihypertrophy, and horseshoe kidney. The syndrome affects both sexes but is more frequent in males. Bibliography: P. Brusa, C. Torricelli:

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