| Oral abnormalities in the Ellis-van Creveld syndrome. | |
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MedLine Citation:
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PMID: 20427928 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Ellis-van Creveld (EvC) syndrome is an autosomal recessive disorder, mainly affecting the ectodermal components such as, enamel, nail, and hair. The gene for EvC syndrome is located on chromosome 4p16. Patients with EvC syndrome characteristically presents with congenitally missing teeth, abnormal frenal attachment, microdontia, and hexadactyly. |
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Authors:
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Prashant Babaji |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Indian journal of dental research : official publication of Indian Society for Dental Research Volume: 21 ISSN: 1998-3603 ISO Abbreviation: Indian J Dent Res Publication Date: 2010 Jan-Mar |
Date Detail:
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Created Date: 2010-04-29 Completed Date: 2010-07-20 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9202990 Medline TA: Indian J Dent Res Country: India |
Other Details:
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Languages: eng Pagination: 143-5 Citation Subset: D |
Affiliation:
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Department of Pedodontics and Preventive Dentistry, SPPGIDMS, Lucknow, Uttar Pradesh, India. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adolescent Anodontia / etiology Consanguinity Ellis-Van Creveld Syndrome / complications* Female Humans Labial Frenum / abnormalities Tooth Abnormalities / etiology* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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