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Bilateral split hand foot malformation in siblings: Case series

INTRODUCTION: Split Hand-Foot malformation (SHFM) is a congenital limb defect that affects the central rays of the hands and/or feet. It is a rare condition that has genetic and environmental etiologies. It ranges in severity depending on the extent of the malformation. We report on two siblings wit...

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Autores principales: Ashi, Mohammed, Assur, Rehab, Awan, Basim, Aljaaly, Hattan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910499/
https://www.ncbi.nlm.nih.gov/pubmed/29499514
http://dx.doi.org/10.1016/j.ijscr.2017.12.030
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author Ashi, Mohammed
Assur, Rehab
Awan, Basim
Aljaaly, Hattan
author_facet Ashi, Mohammed
Assur, Rehab
Awan, Basim
Aljaaly, Hattan
author_sort Ashi, Mohammed
collection PubMed
description INTRODUCTION: Split Hand-Foot malformation (SHFM) is a congenital limb defect that affects the central rays of the hands and/or feet. It is a rare condition that has genetic and environmental etiologies. It ranges in severity depending on the extent of the malformation. We report on two siblings with severe SHFM affecting all limbs. METHODS: We described two cases of siblings with SHFM and discuss the possible causes of the condition. This research did not require ethical approval due to the institute not requiring it for this type of study. RESULTS: Case 1 is a 7-year-old boy, and case 2 is his 4-year-old brother. They are both medically and surgically free. They had normal growth and development and were products of a consanguineous marriage. They both presented with bilateral deformities of the hands and feet, and had no previous family history of congenital anomalies. CONCLUSION: SHFM may occur as a result of consanguineous marriage, genetic mutation, and chemical exposure. Genetic counseling and thorough assessment of associated anomalies is mandatory.
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spelling pubmed-59104992018-04-23 Bilateral split hand foot malformation in siblings: Case series Ashi, Mohammed Assur, Rehab Awan, Basim Aljaaly, Hattan Int J Surg Case Rep Article INTRODUCTION: Split Hand-Foot malformation (SHFM) is a congenital limb defect that affects the central rays of the hands and/or feet. It is a rare condition that has genetic and environmental etiologies. It ranges in severity depending on the extent of the malformation. We report on two siblings with severe SHFM affecting all limbs. METHODS: We described two cases of siblings with SHFM and discuss the possible causes of the condition. This research did not require ethical approval due to the institute not requiring it for this type of study. RESULTS: Case 1 is a 7-year-old boy, and case 2 is his 4-year-old brother. They are both medically and surgically free. They had normal growth and development and were products of a consanguineous marriage. They both presented with bilateral deformities of the hands and feet, and had no previous family history of congenital anomalies. CONCLUSION: SHFM may occur as a result of consanguineous marriage, genetic mutation, and chemical exposure. Genetic counseling and thorough assessment of associated anomalies is mandatory. Elsevier 2017-12-27 /pmc/articles/PMC5910499/ /pubmed/29499514 http://dx.doi.org/10.1016/j.ijscr.2017.12.030 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ashi, Mohammed
Assur, Rehab
Awan, Basim
Aljaaly, Hattan
Bilateral split hand foot malformation in siblings: Case series
title Bilateral split hand foot malformation in siblings: Case series
title_full Bilateral split hand foot malformation in siblings: Case series
title_fullStr Bilateral split hand foot malformation in siblings: Case series
title_full_unstemmed Bilateral split hand foot malformation in siblings: Case series
title_short Bilateral split hand foot malformation in siblings: Case series
title_sort bilateral split hand foot malformation in siblings: case series
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910499/
https://www.ncbi.nlm.nih.gov/pubmed/29499514
http://dx.doi.org/10.1016/j.ijscr.2017.12.030
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