| WAGR syndrome with tetralogy of Fallot and hydrocephalus. | |
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MedLine Citation:
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PMID: 21364466 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Wilms tumor, aniridia, genitourinary abnormalities, and mental retardation (WAGR) syndrome occurs sporadically due to deletion of chromosome 11p13. A variety of other abnormalities involving different systems have been reported in patients with WAGR syndrome. We report on a patient with WAGR syndrome with accompanying tetralogy of Fallot and hydrocephalus. |
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Authors:
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Haci Ahmet Demir; Ali Varan; Eda G Utine; Dilek Aktaş; Berna Oğuz; Dorina Rama; Münevver Büyükpamukçu |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Journal of pediatric hematology/oncology Volume: 33 ISSN: 1536-3678 ISO Abbreviation: J. Pediatr. Hematol. Oncol. Publication Date: 2011 May |
Date Detail:
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Created Date: 2011-04-25 Completed Date: 2011-06-30 Revised Date: 2011-10-06 |
Medline Journal Info:
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Nlm Unique ID: 9505928 Medline TA: J Pediatr Hematol Oncol Country: United States |
Other Details:
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Languages: eng Pagination: e174-5 Citation Subset: IM |
Affiliation:
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Department of Pediatric Oncology, Hacettepe University, Ankara, Turkey. hdemir@hacettepe.edu.tr |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Chromosome Aberrations Chromosomes, Human, Pair 11 Female Humans Hydrocephalus / complications* Infant Mental Retardation / complications* Tetralogy of Fallot / complications* WAGR Syndrome / complications*, genetics |
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