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Congenital syndactyly: a retrospective study of 18 cases at the Department of Orthopaedic Surgery and Traumatology of the Habib Bourguiba University Hospital, Sfax, Tunisia

Congenital syndactylies are frequent congenital malformations of the hand. They can be an isolated finding or they can be found in association with other polymalformative syndromes. Several surgical techniques used to treat them have been described in the literature. The most used is the dorsal comm...

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Autores principales: Guidara, Ahmed Racem, Nizar, Sahnoun, Bardaa, Tarek, Trigui, Moez, Kmiha, Sana, Ayadi, Kamel, Keskes, Hassib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895564/
https://www.ncbi.nlm.nih.gov/pubmed/35291357
http://dx.doi.org/10.11604/pamj.2022.41.30.30253
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author Guidara, Ahmed Racem
Nizar, Sahnoun
Bardaa, Tarek
Trigui, Moez
Kmiha, Sana
Ayadi, Kamel
Keskes, Hassib
author_facet Guidara, Ahmed Racem
Nizar, Sahnoun
Bardaa, Tarek
Trigui, Moez
Kmiha, Sana
Ayadi, Kamel
Keskes, Hassib
author_sort Guidara, Ahmed Racem
collection PubMed
description Congenital syndactylies are frequent congenital malformations of the hand. They can be an isolated finding or they can be found in association with other polymalformative syndromes. Several surgical techniques used to treat them have been described in the literature. The most used is the dorsal commissural omega-flap technique. We here report a study of 18 patients with congenital syndactyly, with multiple involvement in several cases, whose data were collected at the Department of Orthopedics and Traumatology of Sfax (Tunisia). All patients were operated using the dorsal commissural omega-flap technique. We operated 42 commissures in 18 patients. The average age of patients was 7 years. Only 3 patients had syndromic forms. Six of these patients were operated in two stages. For scar quality, mean OSAS score was 11.47 (11.35 for simple types and 12 for complex types). All patients with complex types had long-term complications (100%). Six patients with simple types out of 14 had complications (42.85%). The management of congenital syndactylies is surgical. It is important to provide parents with accurate information on the essential role of follow-up appointments in order to avoid complications in the short and the long term.
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spelling pubmed-88955642022-03-14 Congenital syndactyly: a retrospective study of 18 cases at the Department of Orthopaedic Surgery and Traumatology of the Habib Bourguiba University Hospital, Sfax, Tunisia Guidara, Ahmed Racem Nizar, Sahnoun Bardaa, Tarek Trigui, Moez Kmiha, Sana Ayadi, Kamel Keskes, Hassib Pan Afr Med J Case Series Congenital syndactylies are frequent congenital malformations of the hand. They can be an isolated finding or they can be found in association with other polymalformative syndromes. Several surgical techniques used to treat them have been described in the literature. The most used is the dorsal commissural omega-flap technique. We here report a study of 18 patients with congenital syndactyly, with multiple involvement in several cases, whose data were collected at the Department of Orthopedics and Traumatology of Sfax (Tunisia). All patients were operated using the dorsal commissural omega-flap technique. We operated 42 commissures in 18 patients. The average age of patients was 7 years. Only 3 patients had syndromic forms. Six of these patients were operated in two stages. For scar quality, mean OSAS score was 11.47 (11.35 for simple types and 12 for complex types). All patients with complex types had long-term complications (100%). Six patients with simple types out of 14 had complications (42.85%). The management of congenital syndactylies is surgical. It is important to provide parents with accurate information on the essential role of follow-up appointments in order to avoid complications in the short and the long term. The African Field Epidemiology Network 2022-01-12 /pmc/articles/PMC8895564/ /pubmed/35291357 http://dx.doi.org/10.11604/pamj.2022.41.30.30253 Text en Copyright: Ahmed Racem Guidara et al. https://creativecommons.org/licenses/by/4.0/The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Series
Guidara, Ahmed Racem
Nizar, Sahnoun
Bardaa, Tarek
Trigui, Moez
Kmiha, Sana
Ayadi, Kamel
Keskes, Hassib
Congenital syndactyly: a retrospective study of 18 cases at the Department of Orthopaedic Surgery and Traumatology of the Habib Bourguiba University Hospital, Sfax, Tunisia
title Congenital syndactyly: a retrospective study of 18 cases at the Department of Orthopaedic Surgery and Traumatology of the Habib Bourguiba University Hospital, Sfax, Tunisia
title_full Congenital syndactyly: a retrospective study of 18 cases at the Department of Orthopaedic Surgery and Traumatology of the Habib Bourguiba University Hospital, Sfax, Tunisia
title_fullStr Congenital syndactyly: a retrospective study of 18 cases at the Department of Orthopaedic Surgery and Traumatology of the Habib Bourguiba University Hospital, Sfax, Tunisia
title_full_unstemmed Congenital syndactyly: a retrospective study of 18 cases at the Department of Orthopaedic Surgery and Traumatology of the Habib Bourguiba University Hospital, Sfax, Tunisia
title_short Congenital syndactyly: a retrospective study of 18 cases at the Department of Orthopaedic Surgery and Traumatology of the Habib Bourguiba University Hospital, Sfax, Tunisia
title_sort congenital syndactyly: a retrospective study of 18 cases at the department of orthopaedic surgery and traumatology of the habib bourguiba university hospital, sfax, tunisia
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895564/
https://www.ncbi.nlm.nih.gov/pubmed/35291357
http://dx.doi.org/10.11604/pamj.2022.41.30.30253
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