Cargando…
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...
Autor principal: | |
---|---|
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 |
_version_ | 1783733605607931904 |
---|---|
author | Mubaraki, Adnan A. |
author_facet | Mubaraki, Adnan A. |
author_sort | Mubaraki, Adnan A. |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-8339453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mubarakiadnana nemalinemyopathyacasereport |