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Nemaline Myopathy: A Case Report

Generalized weakness in the pediatric and adolescent population is caused by many disorders that affect the neuromuscular axis. As next-generation sequencing (NGS) is becoming of high yield in replacing more invasive procedures, that is, muscle and nerve biopsy, more previously undiagnosed diseases...

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Autor principal: Mubaraki, Adnan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339453/
https://www.ncbi.nlm.nih.gov/pubmed/34413753
http://dx.doi.org/10.1159/000517898
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author Mubaraki, Adnan A.
author_facet Mubaraki, Adnan A.
author_sort Mubaraki, Adnan A.
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description Generalized weakness in the pediatric and adolescent population is caused by many disorders that affect the neuromuscular axis. As next-generation sequencing (NGS) is becoming of high yield in replacing more invasive procedures, that is, muscle and nerve biopsy, more previously undiagnosed diseases of the muscles are now labeled with specific pathogenicity. A 16-year-old-girl diagnosed with nemaline myopathy but previously was misdiagnosed with congenital myasthenia and put-on unnecessary medications. Clinicians should be aware of congenital diseases that affect the muscles and know the importance of the NGS in reaching the correct diagnosis more so when there is a history of consanguinity.
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spelling pubmed-83394532021-08-18 Nemaline Myopathy: A Case Report Mubaraki, Adnan A. Case Rep Neurol Single Case − General Neurology Generalized weakness in the pediatric and adolescent population is caused by many disorders that affect the neuromuscular axis. As next-generation sequencing (NGS) is becoming of high yield in replacing more invasive procedures, that is, muscle and nerve biopsy, more previously undiagnosed diseases of the muscles are now labeled with specific pathogenicity. A 16-year-old-girl diagnosed with nemaline myopathy but previously was misdiagnosed with congenital myasthenia and put-on unnecessary medications. Clinicians should be aware of congenital diseases that affect the muscles and know the importance of the NGS in reaching the correct diagnosis more so when there is a history of consanguinity. S. Karger AG 2021-07-21 /pmc/articles/PMC8339453/ /pubmed/34413753 http://dx.doi.org/10.1159/000517898 Text en Copyright © 2021 by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Single Case − General Neurology
Mubaraki, Adnan A.
Nemaline Myopathy: A Case Report
title Nemaline Myopathy: A Case Report
title_full Nemaline Myopathy: A Case Report
title_fullStr Nemaline Myopathy: A Case Report
title_full_unstemmed Nemaline Myopathy: A Case Report
title_short Nemaline Myopathy: A Case Report
title_sort nemaline myopathy: a case report
topic Single Case − General Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339453/
https://www.ncbi.nlm.nih.gov/pubmed/34413753
http://dx.doi.org/10.1159/000517898
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