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Vraie macrodactylie avec orientation nerveuse

Real macrodactylia is a rare congenital abnormality of unknown etiology, characterized by excessive growth of the anatomical structures of one or several rays of the hand. It is usually isolated and causes a fibrofatty infiltration mainly involving the palm. It can be caused by embryonic or neurogen...

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Autores principales: Nasri, Siham, Amer, Asmae Oulad, Aichouni, Narjisse, Kamaoui, Imane, Skiker, Imane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457725/
https://www.ncbi.nlm.nih.gov/pubmed/31007808
http://dx.doi.org/10.11604/pamj.2018.31.61.15303
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author Nasri, Siham
Amer, Asmae Oulad
Aichouni, Narjisse
Kamaoui, Imane
Skiker, Imane
author_facet Nasri, Siham
Amer, Asmae Oulad
Aichouni, Narjisse
Kamaoui, Imane
Skiker, Imane
author_sort Nasri, Siham
collection PubMed
description Real macrodactylia is a rare congenital abnormality of unknown etiology, characterized by excessive growth of the anatomical structures of one or several rays of the hand. It is usually isolated and causes a fibrofatty infiltration mainly involving the palm. It can be caused by embryonic or neurogenic abnormalities with or without nerve involvement according to whether macrodactylia has led to an increase in the volume of a major nerve, more often the median. From an evolutionary point of view, it is necessary to distinguish between static macrodactylia (present at birth and remaining stable during growth) and progressive macrodactylia (with a disproportionate growths). Some other syndromes, tumors or abnormalities can cause an increase in finger volume. This abnormality results in functional disability but also in disfigurement. Treatment is based on surgery and rehabilitation.
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spelling pubmed-64577252019-04-19 Vraie macrodactylie avec orientation nerveuse Nasri, Siham Amer, Asmae Oulad Aichouni, Narjisse Kamaoui, Imane Skiker, Imane Pan Afr Med J Case Report Real macrodactylia is a rare congenital abnormality of unknown etiology, characterized by excessive growth of the anatomical structures of one or several rays of the hand. It is usually isolated and causes a fibrofatty infiltration mainly involving the palm. It can be caused by embryonic or neurogenic abnormalities with or without nerve involvement according to whether macrodactylia has led to an increase in the volume of a major nerve, more often the median. From an evolutionary point of view, it is necessary to distinguish between static macrodactylia (present at birth and remaining stable during growth) and progressive macrodactylia (with a disproportionate growths). Some other syndromes, tumors or abnormalities can cause an increase in finger volume. This abnormality results in functional disability but also in disfigurement. Treatment is based on surgery and rehabilitation. The African Field Epidemiology Network 2018-09-27 /pmc/articles/PMC6457725/ /pubmed/31007808 http://dx.doi.org/10.11604/pamj.2018.31.61.15303 Text en © Siham Nasri et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Nasri, Siham
Amer, Asmae Oulad
Aichouni, Narjisse
Kamaoui, Imane
Skiker, Imane
Vraie macrodactylie avec orientation nerveuse
title Vraie macrodactylie avec orientation nerveuse
title_full Vraie macrodactylie avec orientation nerveuse
title_fullStr Vraie macrodactylie avec orientation nerveuse
title_full_unstemmed Vraie macrodactylie avec orientation nerveuse
title_short Vraie macrodactylie avec orientation nerveuse
title_sort vraie macrodactylie avec orientation nerveuse
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457725/
https://www.ncbi.nlm.nih.gov/pubmed/31007808
http://dx.doi.org/10.11604/pamj.2018.31.61.15303
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