| MPPH Syndrome: Two New Cases. | |
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MedLine Citation:
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PMID: 21481746 Owner: NLM Status: In-Data-Review |
Abstract/OtherAbstract:
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This report describes 2 additional cases of megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus syndrome, a recently recognized disorder of infants and young children with macrocrania, developmental delay/mental retardation, and often epilepsy. Medulloblastoma, a previously unreported feature in megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus syndrome, developed in one child at 3 years of age. Although the disorder is presumed to be genetic, the cause of megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus syndrome has not yet been determined. |
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Authors:
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Wendy L Osterling; Richard S Boyer; Gary L Hedlund; James F Bale |
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Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: Pediatric neurology Volume: 44 ISSN: 1873-5150 ISO Abbreviation: Pediatr. Neurol. Publication Date: 2011 May |
Date Detail:
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Created Date: 2011-04-12 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 8508183 Medline TA: Pediatr Neurol Country: United States |
Other Details:
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Languages: eng Pagination: 370-3 Citation Subset: IM |
Copyright Information:
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Copyright © 2011 Elsevier Inc. All rights reserved. |
Affiliation:
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Department of Pediatrics, the University of Utah School of Medicine, Salt Lake City, Utah, and Primary Children's Medical Center, Intermountain Healthcare Inc., Salt Lake City, Utah; Department of Neurology, the University of Utah School of Medicine, Salt Lake City, Utah, and Primary Children's Medical Center, Intermountain Healthcare Inc., Salt Lake City, Utah. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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