Extractions: Anzeige: Verdienen Sie Geld mit Ihren ungenutzten Domains! Welt English Health ... Conditions and Diseases : C A B C D E F G ... Cytomegalovirus This category in other languages: Danish Dutch German Spanish ... Eintrag in weiteren Suchmaschinen Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor In einigen Teilen modifizierte Version des DMOZ.
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/
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
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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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
Extractions: 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.
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
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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.
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
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
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
Extractions: 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 ...
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
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. Aase-Smith syndrome A familial deformity syndrome. Aases 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.
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
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.
