Please use this identifier to cite or link to this item: http://hdl.handle.net/11513/200
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dc.contributor.authorAn, İsa-
dc.contributor.authorAksoy, Mustafa-
dc.date.accessioned2019-06-12T10:34:39Z-
dc.date.available2019-06-12T10:34:39Z-
dc.date.issued2018-
dc.identifier.otherDOI: 10.5455/annalsmedres.2019.01.037-
dc.identifier.urihttp://hdl.handle.net/11513/200-
dc.description.abstractMacrodactyly 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 methodsen_US
dc.language.isoenen_US
dc.publisherAnnals of Medical Researchen_US
dc.titleA case of isolated macrodactylyen_US
dc.typeOtheren_US
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