Cargando…

General Anesthesia in Schwartz-Jampel Syndrome: A Case Report

INTRODUCTION: Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disease characterized by muscle weakness and stiffness, abnormal bone development, short stature, joint contractures, and facial dysmorphisms. Myopathy, anatomical deformities, and malignant hyperthermia are challenging for a...

Descripción completa

Detalles Bibliográficos
Autores principales: Derakhshan, Pooya, Habibi, Azadeh, Amniati, Saied
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brieflands 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664156/
https://www.ncbi.nlm.nih.gov/pubmed/38021333
http://dx.doi.org/10.5812/aapm-129305
_version_ 1785138555156168704
author Derakhshan, Pooya
Habibi, Azadeh
Amniati, Saied
author_facet Derakhshan, Pooya
Habibi, Azadeh
Amniati, Saied
author_sort Derakhshan, Pooya
collection PubMed
description INTRODUCTION: Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disease characterized by muscle weakness and stiffness, abnormal bone development, short stature, joint contractures, and facial dysmorphisms. Myopathy, anatomical deformities, and malignant hyperthermia are challenging for anesthesiologists. CASE PRESENTATION: This case report describes one case of SJS. The female patient was scheduled for Blepharoplasty in Rasuol Akram General Hospital. CONCLUSIONS: These patients may have difficult intubation and be prone to malignant hyperthermia. We managed this patient by applying Rocuronium, propofol, and C-MAC video laryngoscopy.
format Online
Article
Text
id pubmed-10664156
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Brieflands
record_format MEDLINE/PubMed
spelling pubmed-106641562023-03-16 General Anesthesia in Schwartz-Jampel Syndrome: A Case Report Derakhshan, Pooya Habibi, Azadeh Amniati, Saied Anesth Pain Med Case Report INTRODUCTION: Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disease characterized by muscle weakness and stiffness, abnormal bone development, short stature, joint contractures, and facial dysmorphisms. Myopathy, anatomical deformities, and malignant hyperthermia are challenging for anesthesiologists. CASE PRESENTATION: This case report describes one case of SJS. The female patient was scheduled for Blepharoplasty in Rasuol Akram General Hospital. CONCLUSIONS: These patients may have difficult intubation and be prone to malignant hyperthermia. We managed this patient by applying Rocuronium, propofol, and C-MAC video laryngoscopy. Brieflands 2023-03-16 /pmc/articles/PMC10664156/ /pubmed/38021333 http://dx.doi.org/10.5812/aapm-129305 Text en Copyright © 2023, Derakhshan et al. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Case Report
Derakhshan, Pooya
Habibi, Azadeh
Amniati, Saied
General Anesthesia in Schwartz-Jampel Syndrome: A Case Report
title General Anesthesia in Schwartz-Jampel Syndrome: A Case Report
title_full General Anesthesia in Schwartz-Jampel Syndrome: A Case Report
title_fullStr General Anesthesia in Schwartz-Jampel Syndrome: A Case Report
title_full_unstemmed General Anesthesia in Schwartz-Jampel Syndrome: A Case Report
title_short General Anesthesia in Schwartz-Jampel Syndrome: A Case Report
title_sort general anesthesia in schwartz-jampel syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664156/
https://www.ncbi.nlm.nih.gov/pubmed/38021333
http://dx.doi.org/10.5812/aapm-129305
work_keys_str_mv AT derakhshanpooya generalanesthesiainschwartzjampelsyndromeacasereport
AT habibiazadeh generalanesthesiainschwartzjampelsyndromeacasereport
AT amniatisaied generalanesthesiainschwartzjampelsyndromeacasereport