| Japanese family with Greig cephalopolysyndactyly syndrome, including bilateral seven toes, and esotropia, over three generations. | |
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MedLine Citation:
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PMID: 16912002 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We report a Japanese family with Greig cephalopolysyndactyly syndrome (GCPS), in which the grandmother, mother, and daughter were affected. They each had the same characteristics including bilateral seven toes, hypertelorism, and esotropia. Bilateral seven toes and esotropia had followed over three generations and have not previously been reported in this syndrome. The present case with bilateral seven toes and esotropia may be a new type. |
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Authors:
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Gan Muneuchi; Shigehiko Suzuki; Miki Sato; Motoki Tamai; Hiroharu H Igawa |
Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Scandinavian journal of plastic and reconstructive surgery and hand surgery / Nordisk plastikkirurgisk forening [and] Nordisk klubb for handkirurgi Volume: 40 ISSN: 0284-4311 ISO Abbreviation: Scand J Plast Reconstr Surg Hand Surg Publication Date: 2006 |
Date Detail:
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Created Date: 2006-08-16 Completed Date: 2007-01-09 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 8707869 Medline TA: Scand J Plast Reconstr Surg Hand Surg Country: Sweden |
Other Details:
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Languages: eng Pagination: 253-6 Citation Subset: IM |
Affiliation:
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Department of Plastic and Reconstructive Surgery, Kagawa University, Kagawa, Japan. muneuchi@med.kagawa-u.ac.jp |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adult Asian Continental Ancestry Group / genetics Craniofacial Abnormalities / genetics* Esotropia / genetics* Female Humans Infant Pedigree Polydactyly / genetics* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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