Freeman-Sheldon syndrome. A case report and review of the literature.
La Chirurgia degli organi di movimento, ISSN: 1973-2538, Vol: 92, Issue: 2, Page: 127-131
2008
- 11Citations
- 37Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations11
- Citation Indexes11
- 11
- CrossRef8
- Captures37
- Readers37
- 37
Review Description
The Authors describe a case of Freeman-Sheldon Syndrome, a rare congenital autosomal dominant disorder (gene mapped on chromosome 11p15.5) characterized by microstomia with crinkled lips, camptodactyly with ulnar deviation of the fingers and equinus-varus-supine clubfoot. The autosomal recessive form, even rarer and difficult to recognize, has a more severe clinical manifestation. The symptomatology is worsened by breathing and swallowing disorders due to the small orifices of the mouth and nose, which sometimes require tracheotomy to avoid obstruction of the airways.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=60749088043&origin=inward; http://dx.doi.org/10.1007/s12306-008-0053-4; http://www.ncbi.nlm.nih.gov/pubmed/18677448; http://link.springer.com/10.1007/s12306-008-0053-4; http://www.springerlink.com/index/10.1007/s12306-008-0053-4; http://www.springerlink.com/index/pdf/10.1007/s12306-008-0053-4; https://dx.doi.org/10.1007/s12306-008-0053-4; https://link.springer.com/article/10.1007/s12306-008-0053-4
Springer Science and Business Media LLC
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