A rare case of unilateral postaxial duplicated foot in a developmentally normal child

Diplopodia, being a rare congenital disorder, is infrequently discussed in published texts. Most reported cases have accounted the involvement of duplicated preaxial digits with other associated organ system and physical deformities. Here, we present an unusual case of isolated diplopodia involving...

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Main Authors: Haniza, Sahdi, Hoong, Chan Wai, Ahmad Hata, Rasit, Arianto, Fredy, Siong, Lau Kiew, Nur Alyana Benjamin, Abdullah
Format: Article
Language:English
Published: Hong Kong Academy of Medicine Press 2017
Subjects:
Online Access:http://ir.unimas.my/id/eprint/19161/
http://ir.unimas.my/id/eprint/19161/2/A%20rare%20case.pdf
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author Haniza, Sahdi
Hoong, Chan Wai
Ahmad Hata, Rasit
Arianto, Fredy
Siong, Lau Kiew
Nur Alyana Benjamin, Abdullah
author_facet Haniza, Sahdi
Hoong, Chan Wai
Ahmad Hata, Rasit
Arianto, Fredy
Siong, Lau Kiew
Nur Alyana Benjamin, Abdullah
author_sort Haniza, Sahdi
building UNIMAS Institutional Repository
collection Online Access
description Diplopodia, being a rare congenital disorder, is infrequently discussed in published texts. Most reported cases have accounted the involvement of duplicated preaxial digits with other associated organ system and physical deformities. Here, we present an unusual case of isolated diplopodia involving postaxial toes in a child with no other organ and physical abnormalities. Radiological studies revealed a set of 10-digit-duplicated foot over the lateral aspect of the native foot, complete with phalanges and its corresponding metatarsals as well as tarsals, supplied by an anomalous posterior branch of the popliteal artery. Definitive surgery was performed just before the child was learning to walk.
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spelling unimas-191612023-08-23T01:50:56Z http://ir.unimas.my/id/eprint/19161/ A rare case of unilateral postaxial duplicated foot in a developmentally normal child Haniza, Sahdi Hoong, Chan Wai Ahmad Hata, Rasit Arianto, Fredy Siong, Lau Kiew Nur Alyana Benjamin, Abdullah RD Surgery Diplopodia, being a rare congenital disorder, is infrequently discussed in published texts. Most reported cases have accounted the involvement of duplicated preaxial digits with other associated organ system and physical deformities. Here, we present an unusual case of isolated diplopodia involving postaxial toes in a child with no other organ and physical abnormalities. Radiological studies revealed a set of 10-digit-duplicated foot over the lateral aspect of the native foot, complete with phalanges and its corresponding metatarsals as well as tarsals, supplied by an anomalous posterior branch of the popliteal artery. Definitive surgery was performed just before the child was learning to walk. Hong Kong Academy of Medicine Press 2017 Article PeerReviewed text en http://ir.unimas.my/id/eprint/19161/2/A%20rare%20case.pdf Haniza, Sahdi and Hoong, Chan Wai and Ahmad Hata, Rasit and Arianto, Fredy and Siong, Lau Kiew and Nur Alyana Benjamin, Abdullah (2017) A rare case of unilateral postaxial duplicated foot in a developmentally normal child. Journal of Orthopaedic Surgery, 25 (1). pp. 1-7. ISSN 2309-4990 http://doi.org/10.1177/2309499016684989 doi:10.1177/2309499016684989
spellingShingle RD Surgery
Haniza, Sahdi
Hoong, Chan Wai
Ahmad Hata, Rasit
Arianto, Fredy
Siong, Lau Kiew
Nur Alyana Benjamin, Abdullah
A rare case of unilateral postaxial duplicated foot in a developmentally normal child
title A rare case of unilateral postaxial duplicated foot in a developmentally normal child
title_full A rare case of unilateral postaxial duplicated foot in a developmentally normal child
title_fullStr A rare case of unilateral postaxial duplicated foot in a developmentally normal child
title_full_unstemmed A rare case of unilateral postaxial duplicated foot in a developmentally normal child
title_short A rare case of unilateral postaxial duplicated foot in a developmentally normal child
title_sort rare case of unilateral postaxial duplicated foot in a developmentally normal child
topic RD Surgery
url http://ir.unimas.my/id/eprint/19161/
http://ir.unimas.my/id/eprint/19161/
http://ir.unimas.my/id/eprint/19161/
http://ir.unimas.my/id/eprint/19161/2/A%20rare%20case.pdf