| Two cases of Walker-Warburg syndrome complicated by hydrocephalus. | |
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MedLine Citation:
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PMID: 20516736 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Walker-Warburg syndrome is a very rare autosomal recessive disorder with congenital muscular dystrophy, brain malformations on the basis of a neuronal migration defect and ocular abnormalities. We report our experience in treating two cases of Walker-Warburg syndrome complicated by hydrocephalus with shunting and endoscopic techniques. |
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Authors:
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M Preuss; M Heckmann; M Stein; U Nestler |
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Publication Detail:
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Type: Case Reports; Journal Article Date: 2010-05-27 |
Journal Detail:
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Title: Pediatric neurosurgery Volume: 46 ISSN: 1423-0305 ISO Abbreviation: Pediatr Neurosurg Publication Date: 2010 |
Date Detail:
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Created Date: 2010-06-16 Completed Date: 2010-09-22 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9114967 Medline TA: Pediatr Neurosurg Country: Switzerland |
Other Details:
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Languages: eng Pagination: 34-8 Citation Subset: IM |
Copyright Information:
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Copyright 2010 S. Karger AG, Basel. |
Affiliation:
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Department of Neurosurgery, University Hospital Giessen, Giessen, Germany. preuss@neurosurgeon.ch |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Abnormalities, Multiple* Brain / abnormalities*, pathology Endoscopy Female Follow-Up Studies Humans Hydrocephalus* / complications, pathology, surgery Infant, Newborn Magnetic Resonance Imaging Male Muscular Dystrophies / complications*, congenital Neurosurgical Procedures Syndrome* Ventriculoperitoneal Shunt* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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