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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Hocaoglu, Emre Berköz, Ömer Dogan, Yunus Özkan, Türker |
| Description | Author Affiliation: Hocaoglu E ( Specialist, Department of Plastic Reconstructive and Aesthetic Surgery, Istanbul University Faculty of Medicine, Istanbul, Turkey. Electronic address: emrehocaoglu@gmail.com.) |
| Abstract | Diplopodia is a rare congenital anomaly and has been described as extra digits, metatarsals, and tarsal bones that form an extra foot or foot-like structure. Various skeletal deformities and anomalies involving other organ systems can accompany diplopodia. Treatment consists of surgery, splinting, and physical therapy, planned according to each patient's specific condition. We present a patient who had diplopodia with distinctive anatomic features (with postaxial polydactyly and without any anomaly of the tibia or fibula) compared with the previously reported cases, and concomitant anomalies, including left renal agenesis and anal atresia. |
| File Format | HTM / HTML |
| ISSN | 10672516 |
| Issue Number | 6 |
| Journal | The Journal of Foot and Ankle Surgery |
| Volume Number | 52 |
| e-ISSN | 15422224 |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2013-11-01 |
| Publisher Place | United States |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Discipline Orthopedics Discipline General Surgery Foot Deformities, Congenital Surgery Polydactyly Humans Infant, Newborn Male Metatarsal Bones Abnormalities Case Reports Journal Article |
| Content Type | Text |
| Resource Type | Case study Article |
| Subject | Orthopedics and Sports Medicine Surgery |
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