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 |