AllRefer Health - Medical Encyclopedia - N Nephritis Syndrome Acute (Acute Nephritic Syndrome); nephroblastoma (Wilms Tumor) Nephrogenic Diabetes Insipidus - congenital (congenital Nephrogenic http://health.allrefer.com/health/health-topics-n.html
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Publications Biomédicales De Rouen : Mai 1997 A oneyear old girl with congenital aniridia was admitted for macroscopic hematuria . CONCLUSION Both cases of fetal rhabdomyomatous nephroblastoma, http://www.chu-rouen.fr/drrc/pub/pub9705.html
Extractions: <0.000001). All patients (16/16) presenting with multiple tumours had at least one positive biopsy, compared with only 53% (19/36) of patients presenting with single tumours (P <0.001). This defines expansion of multiple clones of mutant p53-containing cells as an important biological mechanism of field cancerisation, and provides a means to identify patients likely to benefit from intensive screening for the development of new head and neck tumours.
Results Of The Search A pathological study of nephroblastoma with congenital aniridia. Combinationof nephroblastoma and aniridia in a child with congenital deletion of http://invention.swmed.edu/trite/abstracts/user-1015659130/results.shtml
Wilms Tumor Solid Tumor. Wilms Tumor. Alternative Names nephroblastoma Congenitalabnormalities It is well documented that certain syndromes, or clusters of http://www.stjude.org/disease-summaries/0,2557,449_2167_2997,00.html
Extractions: @import url(/StJude/CDA/Common/CSS/default.css); @import url(/StJude/CDA/Common/CSS/default_lists.css); @import url(/StJude/CDA/Common/CSS/default_content_types.css); @import url(/StJude/Common/CSS/St_Jude_Clinical_Science); The following browsers support numerous web standards including CSS, XHTML, and the DOM (a universal means of controlling the behavior of web pages): St. Jude Children's Research Hospital Home Clinical Science Home Disease Information Solid Tumors Related Topics Alternative Names: nephroblastoma Wilms tumor is a solid tumor of the kidney that arises from immature kidney cells.
Brusa-Torricelli Syndrome (www.whonamedit.com) BrusaTorricelli syndrome A congenital syndrome in which aniridia andnephroblastoma (Wilms tumour) is associated with multiple abnormalities. http://www.whonamedit.com/synd.cfm/2404.html
Extractions: 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. 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. Since the early 1980s this disorder has commonly been referred to as WAGR syndrome.
Medical Dictionary: C - CureResearch.com congenital heart conditions congenital immunodeficiency congenitalnephroblastoma congenital Spinal Muscular Atrophy with arthrogryposis http://www.cureresearch.com/lists/dictc.htm
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HalfthePlanet Is The Authoritative Online Source Of Reliable Tools congenital Facial Diplegia@ (5); congenital Heart Disease@ (49); congenitalNephroblastoma@ (4); congenital Pain Insensitivity@ (1) http://www.halftheplanet.org/cgi-bin/resources/apexec.pl?etype=odp&passurl=/Heal
Accessing Article She presented with aniridia, cataract, nystagmus, corneal ulcers and bilateralcongenital ptosis. A left nephroblastoma was detected at 15 months. http://www.nature.com/ejhg/journal/v13/n4/full/5201358a.html
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Extractions: NORMAL SONOGRAPHIC ANATOMY Normal development of the anterior abdominal wall depends on the fusion of four ectomesodermic folds (cephalic, caudal and two lateral). At 810 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 1012 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.
601224 POTOCKI-SHAFFER SYNDROME presented with aniridia, cataract, nystagmus, corneal ulcers, and bilateralcongenital ptosis. A left nephroblastoma was detected at 15 months of age. http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:601224] -e
DaytonDailyNews: Dayton, Ohio, News And Information nephroblastoma; Kidney tumor. Definition It is associated with certaincongenital defects including urinary tract abnormalities, absence of the iris http://www.daytondailynews.com/health/healthfd/shared/health/adam/ency/article/0
Extractions: Ency. home Disease W Wilm's tumor See images Overview Symptoms Treatment Alternative names: Nephroblastoma; Kidney tumor Definition: Wilm's tumor is a cancerous tumor of the kidney that occurs in children. Causes and Risks Wilm's tumor is one of the most common intraabdominal tumors in children and the most common type of kidney tumor. The exact cause of tumor formation is unknown, but it probably develops in fetal tissue. It is associated with certain congenital defects including urinary tract abnormalities, absence of the iris (aniridia) and hemihypertrophy (enlargement of one side of the body), and shows an increased incidence among siblings and twins, which suggests a possible genetic cause. The tumor may become quite large, but usually remains encapsulated (self-enclosed). It may spread to other body tissues.
AR Online » Case Reports » CT » Multilocular Cystic Nephroma The differential diagnosis of this lesion includes a cystic partially differentiatednephroblastoma (predominantly cystic Wilms tumor), and congenital http://www.appliedradiology.com/case/case.asp?Id=504&IssueID=2&CatID=29&SubCatID
