| Arthrogryposis multiplex congenita as part of an inherited symptom complex: two case reports and a review of the literature. | |
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MedLine Citation:
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PMID: 643415 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Two first cousins appear to have an autosomal recessive disorder consisting of arthrogryposis multiplex congenita (AMC), pterygium coli, congenital cervical spine fusions, and some features of the Eagle-Barrett syndrome. A review of the literature is summarized including the broad concepts of AMC as well as some syndromes in which AMC is but one manifestation. |
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Authors:
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R C Beckerman; J J Buchino |
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Publication Detail:
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Type: Case Reports; Journal Article; Research Support, U.S. Gov't, Non-P.H.S. |
Journal Detail:
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Title: Pediatrics Volume: 61 ISSN: 0031-4005 ISO Abbreviation: Pediatrics Publication Date: 1978 Mar |
Date Detail:
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Created Date: 1978-06-12 Completed Date: 1978-06-12 Revised Date: 2006-11-15 |
Medline Journal Info:
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Nlm Unique ID: 0376422 Medline TA: Pediatrics Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 417-22 Citation Subset: AIM; IM |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Arthrogryposis
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complications,
genetics* Female Humans Klippel-Feil Syndrome / complications Male Phenotype Pregnancy Pterygium / complications |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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