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         Congenital Nephroblastoma:     more detail

81. AllRefer Health - Medical Encyclopedia - N
Nephritis Syndrome Acute (Acute Nephritic Syndrome); nephroblastoma (Wilms Tumor) Nephrogenic Diabetes Insipidus - congenital (congenital Nephrogenic
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82. 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
Medline - Mai 1997 (N=53) Menu Publications CHU

    Authors

    Alves G. Thiebot J. Tracqui A. Delangre T. Guedon C. Lerebours E.
    Title
    Neurologic disorders due to brain manganese deposition in a jaundiced patient receiving long-term parenteral nutrition.
    Source
    Abstract
    Authors

    Waridel F. Estreicher A. Bron L. Flaman JM. Fontolliet C. Monnier P. Frebourg T. Iggo R.
    Title
    Field cancerisation and polyclonal p53 mutation in the upper aero-digestive tract. Source Oncogene. 14(2):163-9, 1997 Jan 16. Abstract <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. Authors Benichou J. Byrne C. Gail M.

83. 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

New This Month
New This Year Abstract TRITE Statistics Results - FULL MEDLINE:
Aniridia (PAX6(+/-)).
David S Walton J Pediatr Ophthalmol Strabismus 2005 Mar-Apr;42(2);128.

Score: 0.794
Nephroblastoma.
Med J Aust 1977 May;1(20);729-30.

Score: 0.729
PAX6 mutations in aniridia.
I M Hanson ... V van Heyningen Hum Mol Genet 1993 Jul;2(7);915-20.

Score: 0.698
Aniridia and wilms's tumour (nephroblastoma).
T F Mackintosh ... I M Strachan Br J Ophthalmol 1968 Nov;52(11);846-8.

Score: 0.689
A new PAX6 mutation in familial aniridia.
I Hanson ... V van Heyningen J Med Genet 1995 Jun;32(6);488-9.

Score: 0.666
Del11p13/nephroblastoma without aniridia.
C Turleau ... C Junien Hum Genet 1984 ;67(4);455-6.

Score: 0.660
Aniridia: recent achievements in paediatric practice.
I Ivanov ... R Weitz Eur J Pediatr 1995 Oct;154(10);795-800.

Score: 0.658
PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation.
A Malandrini ... A Renieri Clin Genet 2001 Aug;60(2);151-4.

Score: 0.632
Aniridia and essential atrophy of the iris.
D C MACDIARMID

Score: 0.620

84. 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
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Disease Information
Solid Tumor : Wilms Tumor
Alternative Names: nephroblastoma
Definition
  • Wilms tumor is a solid tumor of the kidney that arises from immature kidney cells.

85. 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

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Brusa-Torricelli syndrome Also known as: Aniridia-Wilms’ tumour syndrome Aniridia-Wilms' tumor association Miller’s syndrome (Robert W. Miller) Synonyms: Aniridia-nephroblastoma syndrome, oculocerebrorenal syndrome. Associated persons: P. Brusa Robert 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. Since the early 1980s this disorder has commonly been referred to as WAGR syndrome. We thank Kelly Trout of the International WAGR Syndrome Association for for information submitted.

86. JustCan.com Disability Directory
congenital Facial Diplegia@ (5); congenital Heart Disease@ (41); congenitalNephroblastoma@ (4); congenital Pain Insensitivity@ (1)
http://directory.justcan.com/odpphp/odp.php?browse=/Health/Conditions_and_Diseas

87. 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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  • 88. HalfthePlanet Is The Authoritative Online Source Of Reliable Tools
    congenital Facial Diplegia@ (5); congenital Heart Disease@ (49); congenitalNephroblastoma@ (4); congenital Pain Insensitivity@ (1)
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    89. 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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    90. Anterior Abdominal Wall - DIAGNOSIS OF CONGENITAL ABNORMALITIES - THE 18-23 WEEK
    About 5% of affected individuals develop tumors during childhood, most commonlynephroblastoma 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.

    91. 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

    92. 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
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    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.
    The frequency of disease occurrence is estimated to be about 1 out of 200,000 to 250,000 children. The peak incidence is at 3 years old. Rarely, the tumor may be present in adults.

    93. AR Online » Case Reports » CT » Multilocular Cystic Nephroma
    The differential diagnosis of this lesion includes a cystic partially differentiatednephroblastoma (predominantly cystic Wilm’s tumor), and congenital
    http://www.appliedradiology.com/case/case.asp?Id=504&IssueID=2&CatID=29&SubCatID

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