| An unusual association of intracranial aneurysms and oesophageal duplication in a case of Klippel-Trenaunay syndrome. | |
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MedLine Citation:
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PMID: 11198216 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The Klippel-Trenaunay syndrome (KTS) is a congenital disorder resulting from a mesodermal abnormality, characterised by cutaneous capillary haemangiomas, hypertrophy of bone and soft tissues and varicose veins. The presence of intracranial aneurysms has rarely been described, while oesophageal duplication has not been reported previously. We describe a patient with the KTS with both there additional abnormalities, which could be explained by a postulated mosaic gene abnormality. |
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Authors:
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R De Blasi; A Zenzola; C M Lanzilotti; M Resta; O Caputi; P Lamberti; F Simone; M T Pangrazio; A Carella |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Neuroradiology Volume: 42 ISSN: 0028-3940 ISO Abbreviation: Neuroradiology Publication Date: 2000 Dec |
Date Detail:
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Created Date: 2001-01-25 Completed Date: 2001-03-08 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 1302751 Medline TA: Neuroradiology Country: Germany |
Other Details:
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Languages: eng Pagination: 930-2 Citation Subset: IM |
Affiliation:
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Department of Neuroradiology, University of Bari, Italy. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple* Adult Esophagus / abnormalities* Humans Intracranial Aneurysm / genetics, pathology* Klippel-Trenaunay-Weber Syndrome / complications*, genetics, pathology Magnetic Resonance Imaging Male |
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