A rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult male
Congenital brachymetatarsia is a rare skeletal anomaly which is characterized by the abnormal length reduction of one or more metatarsal bones. It occurs as the result of the early closure of the growth plate. While the majority of the reported cases are idiopathic, it can also be seen in associatio...
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doaj-bf6709b3436e40e4b09ea577c19118b42020-11-24T22:19:25ZengElsevierRadiology Case Reports1930-04332019-10-01141012521254A rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult maleMeltem Özdemir, MD0Rasime Pelin Kavak, MD1Tuba Akdağ, MD2Corresponding author.; Department of Radiology, University of Health Sciences, Dışkapı Yıldırım Beyazıt Training and Research Hospital, Radyoloji Kliniği, Ziraat mah. Şehit Ömer Halisdemir cad. No:20, Altındağ, Ankara, TurkeyDepartment of Radiology, University of Health Sciences, Dışkapı Yıldırım Beyazıt Training and Research Hospital, Radyoloji Kliniği, Ziraat mah. Şehit Ömer Halisdemir cad. No:20, Altındağ, Ankara, TurkeyDepartment of Radiology, University of Health Sciences, Dışkapı Yıldırım Beyazıt Training and Research Hospital, Radyoloji Kliniği, Ziraat mah. Şehit Ömer Halisdemir cad. No:20, Altındağ, Ankara, TurkeyCongenital brachymetatarsia is a rare skeletal anomaly which is characterized by the abnormal length reduction of one or more metatarsal bones. It occurs as the result of the early closure of the growth plate. While the majority of the reported cases are idiopathic, it can also be seen in association with various genetic conditions or syndromes. Brachymetatarsia most commonly involves the fourth metatarsal followed by the first metatarsal. This rare disorder is mostly bilateral and reported almost exclusively in females. Herein, we present a rare case of congenital unilateral brachymetatarsia which was incidentally detected in a young adult male. Keywords: Brachymetatarsia, Short toe, Congenital, Deformityhttp://www.sciencedirect.com/science/article/pii/S1930043319302602 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Meltem Özdemir, MD Rasime Pelin Kavak, MD Tuba Akdağ, MD |
spellingShingle |
Meltem Özdemir, MD Rasime Pelin Kavak, MD Tuba Akdağ, MD A rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult male Radiology Case Reports |
author_facet |
Meltem Özdemir, MD Rasime Pelin Kavak, MD Tuba Akdağ, MD |
author_sort |
Meltem Özdemir, MD |
title |
A rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult male |
title_short |
A rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult male |
title_full |
A rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult male |
title_fullStr |
A rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult male |
title_full_unstemmed |
A rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult male |
title_sort |
rare case of isolated congenital unilateral brachymetatarsia presenting in a young adult male |
publisher |
Elsevier |
series |
Radiology Case Reports |
issn |
1930-0433 |
publishDate |
2019-10-01 |
description |
Congenital brachymetatarsia is a rare skeletal anomaly which is characterized by the abnormal length reduction of one or more metatarsal bones. It occurs as the result of the early closure of the growth plate. While the majority of the reported cases are idiopathic, it can also be seen in association with various genetic conditions or syndromes. Brachymetatarsia most commonly involves the fourth metatarsal followed by the first metatarsal. This rare disorder is mostly bilateral and reported almost exclusively in females. Herein, we present a rare case of congenital unilateral brachymetatarsia which was incidentally detected in a young adult male. Keywords: Brachymetatarsia, Short toe, Congenital, Deformity |
url |
http://www.sciencedirect.com/science/article/pii/S1930043319302602 |
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