Ischiospinal Dysostosis in a Child with Pierre-Robin Syndrome

Ischiospinal Dysostosis (ISD) is a complex and very rare medical entity. It is associated with kyphoscoliosis, dysplasia or aplasia of the ischial rami, segmental anomalies of the bony vertebrae, and peculiar facial morphologies. In this case report, we present a child with Ischiospinal Dysostosis a...

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Autores principales: Almasri, Mahmoud, Kishta, Waleed, Abduljabbar, Fahad H., Arlet, Vincent, Saran, Neil, Oullet, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394385/
https://www.ncbi.nlm.nih.gov/pubmed/28473936
http://dx.doi.org/10.1155/2017/8263536
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author Almasri, Mahmoud
Kishta, Waleed
Abduljabbar, Fahad H.
Arlet, Vincent
Saran, Neil
Oullet, Jean
author_facet Almasri, Mahmoud
Kishta, Waleed
Abduljabbar, Fahad H.
Arlet, Vincent
Saran, Neil
Oullet, Jean
author_sort Almasri, Mahmoud
collection PubMed
description Ischiospinal Dysostosis (ISD) is a complex and very rare medical entity. It is associated with kyphoscoliosis, dysplasia or aplasia of the ischial rami, segmental anomalies of the bony vertebrae, and peculiar facial morphologies. In this case report, we present a child with Ischiospinal Dysostosis and Pierre-Robin Syndrome. This case report is unique as we followed the patient for 13 years in which he had multiple spinal procedures to treat his kyphoscoliosis. In this paper, we elucidated the number of case reports with documented follow-up regarding spinal cord injury or other complications of ISD and its management.
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spelling pubmed-53943852017-05-04 Ischiospinal Dysostosis in a Child with Pierre-Robin Syndrome Almasri, Mahmoud Kishta, Waleed Abduljabbar, Fahad H. Arlet, Vincent Saran, Neil Oullet, Jean Case Rep Orthop Case Report Ischiospinal Dysostosis (ISD) is a complex and very rare medical entity. It is associated with kyphoscoliosis, dysplasia or aplasia of the ischial rami, segmental anomalies of the bony vertebrae, and peculiar facial morphologies. In this case report, we present a child with Ischiospinal Dysostosis and Pierre-Robin Syndrome. This case report is unique as we followed the patient for 13 years in which he had multiple spinal procedures to treat his kyphoscoliosis. In this paper, we elucidated the number of case reports with documented follow-up regarding spinal cord injury or other complications of ISD and its management. Hindawi 2017 2017-04-03 /pmc/articles/PMC5394385/ /pubmed/28473936 http://dx.doi.org/10.1155/2017/8263536 Text en Copyright © 2017 Mahmoud Almasri et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under 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
Almasri, Mahmoud
Kishta, Waleed
Abduljabbar, Fahad H.
Arlet, Vincent
Saran, Neil
Oullet, Jean
Ischiospinal Dysostosis in a Child with Pierre-Robin Syndrome
title Ischiospinal Dysostosis in a Child with Pierre-Robin Syndrome
title_full Ischiospinal Dysostosis in a Child with Pierre-Robin Syndrome
title_fullStr Ischiospinal Dysostosis in a Child with Pierre-Robin Syndrome
title_full_unstemmed Ischiospinal Dysostosis in a Child with Pierre-Robin Syndrome
title_short Ischiospinal Dysostosis in a Child with Pierre-Robin Syndrome
title_sort ischiospinal dysostosis in a child with pierre-robin syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394385/
https://www.ncbi.nlm.nih.gov/pubmed/28473936
http://dx.doi.org/10.1155/2017/8263536
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