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A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report
Merosin-deficient muscular dystrophy is caused by an autosomal recessive mutation on laminin-..2 gene characterized by severe progressive muscle weakness associated with neuromuscular scoliosis and restrictive lung disease. In this case report, we describe an alternative airway approach performed in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533962/ https://www.ncbi.nlm.nih.gov/pubmed/33895222 http://dx.doi.org/10.1016/j.bjane.2021.03.018 |
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author | Pelicano Paulos, Jorge Artilheiro, Vanessa Cruz, Catarina Carneiro, Ana Pinto |
author_facet | Pelicano Paulos, Jorge Artilheiro, Vanessa Cruz, Catarina Carneiro, Ana Pinto |
author_sort | Pelicano Paulos, Jorge |
collection | PubMed |
description | Merosin-deficient muscular dystrophy is caused by an autosomal recessive mutation on laminin-..2 gene characterized by severe progressive muscle weakness associated with neuromuscular scoliosis and restrictive lung disease. In this case report, we describe an alternative airway approach performed in a child with anticipated difficult airway and merosin-deficient muscular dystrophy. Significant anesthetic implications may increase the perioperative risk, requiring accurate knowledge to anticipate an adequate management and provide patient-safety strategies. |
format | Online Article Text |
id | pubmed-10533962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105339622023-09-29 A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report Pelicano Paulos, Jorge Artilheiro, Vanessa Cruz, Catarina Carneiro, Ana Pinto Braz J Anesthesiol Case Reports Merosin-deficient muscular dystrophy is caused by an autosomal recessive mutation on laminin-..2 gene characterized by severe progressive muscle weakness associated with neuromuscular scoliosis and restrictive lung disease. In this case report, we describe an alternative airway approach performed in a child with anticipated difficult airway and merosin-deficient muscular dystrophy. Significant anesthetic implications may increase the perioperative risk, requiring accurate knowledge to anticipate an adequate management and provide patient-safety strategies. Elsevier 2021-04-22 /pmc/articles/PMC10533962/ /pubmed/33895222 http://dx.doi.org/10.1016/j.bjane.2021.03.018 Text en © 2021 Sociedade Brasileira de Anestesiologia. Published by Elsevier Editora Ltda. https://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 | Case Reports Pelicano Paulos, Jorge Artilheiro, Vanessa Cruz, Catarina Carneiro, Ana Pinto A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report |
title | A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report |
title_full | A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report |
title_fullStr | A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report |
title_full_unstemmed | A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report |
title_short | A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report |
title_sort | difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533962/ https://www.ncbi.nlm.nih.gov/pubmed/33895222 http://dx.doi.org/10.1016/j.bjane.2021.03.018 |
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