| An infant with congenital fibula deficiency accompanying with deafness. | |
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MedLine Citation:
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PMID: 23090811 Owner: NLM Status: In-Process |
Abstract/OtherAbstract:
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Congenital longitudinal deficiency of the fibula (CLDF) is the most common congenital defect involving the long bones. There have been many different classifications developed for fibula deficiency. Achterman and Kalamchi's classification is most commonly used and will be described. Our case was complied with type II. Other anomalies includes cardiac anomalies, thrombocytopenia absent-radius (TAR) syndrome, thoracoabdominal schisis, spina bifida and renal anomalies, but most associated anomalies are skeletal. We here presented firstly in literature an infant with congenital fibula deficiency accompanying with deafness. |
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Authors:
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F Cekmez; O Pirgon; F E Canpolat |
Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: European review for medical and pharmacological sciences Volume: 16 Suppl 4 ISSN: 1128-3602 ISO Abbreviation: Eur Rev Med Pharmacol Sci Publication Date: 2012 Oct |
Date Detail:
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Created Date: 2012-10-23 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9717360 Medline TA: Eur Rev Med Pharmacol Sci Country: Italy |
Other Details:
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Languages: eng Pagination: 62-3 Citation Subset: IM |
Affiliation:
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Department of Pediatrics, Gülhane Military Medical Academy, Istanbul. ferhat_cocuk@hotmail.com |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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