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http://hdl.handle.net/11513/200
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | An, İsa | - |
dc.contributor.author | Aksoy, Mustafa | - |
dc.date.accessioned | 2019-06-12T10:34:39Z | - |
dc.date.available | 2019-06-12T10:34:39Z | - |
dc.date.issued | 2018 | - |
dc.identifier.other | DOI: 10.5455/annalsmedres.2019.01.037 | - |
dc.identifier.uri | http://hdl.handle.net/11513/200 | - |
dc.description.abstract | Macrodactyly can be used synonymously with megalodactyly or digital gigantism. It is characterized by the congenitally large formation of one or more fingers of the hand or foot. Macrodactyly is a rare anomaly. There is a growth in the affected soft tissue and bone. It can clinically cause pain and loss of function, stiffness, finger-tip ulceration, carpal tunnel syndrome in hand (1). Patients diagnosed with macrodactyly should be screened for diseases such as Milroy’s disease, Proteus syndrome and Klippel-Trenaunnay-Weber syndrome. Diagnosis and treatment planning are performed by imaging methods | en_US |
dc.language.iso | en | en_US |
dc.publisher | Annals of Medical Research | en_US |
dc.title | A case of isolated macrodactyly | en_US |
dc.type | Other | en_US |
Appears in Collections: | Dahili Tıp Bilimleri Bölümü |
Files in This Item:
File | Description | Size | Format | |
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14. A case of isolated macrodactyly.pdf | 1.02 MB | Adobe PDF | View/Open |
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