Cargando…
Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T
Left ventricular hypertrabeculation/noncompaction is a myocardial abnormality of unknown etiology/pathogenesis, which is frequently associated with neuromuscular disorders or chromosomal defects. LVHT in association with a MYOT mutation has not been reported. The patient is a 72-year-old male with a...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244945/ https://www.ncbi.nlm.nih.gov/pubmed/32509353 http://dx.doi.org/10.1155/2020/5128069 |
_version_ | 1783537663082496000 |
---|---|
author | Finsterer, Josef Stöllberger, Claudia Hasun, Matthias Riedhammer, Korbinian Wagner, Mathias |
author_facet | Finsterer, Josef Stöllberger, Claudia Hasun, Matthias Riedhammer, Korbinian Wagner, Mathias |
author_sort | Finsterer, Josef |
collection | PubMed |
description | Left ventricular hypertrabeculation/noncompaction is a myocardial abnormality of unknown etiology/pathogenesis, which is frequently associated with neuromuscular disorders or chromosomal defects. LVHT in association with a MYOT mutation has not been reported. The patient is a 72-year-old male with a history of strabismus in childhood, asymptomatic creatine-kinase elevation since age 42 years, slowly progressive lower limb weakness since age 60 years, slowly progressive dysarthria and dysphagia since age 62 years, and recurrent episodes of arthralgias and myalgias since age 71 years. He also had arterial hypertension, diverticulosis, hyperlipidemia, coronary heart disease, and a hiatal hernia with reflux esophagitis. Clinical exam revealed mild quadruparesis and proximal wasting of the legs. Whole exome sequencing revealed a known variant in the MYOT gene. Muscle biopsy, previously assessed as inclusion body myopathy, was compatible with the genotype after revision. Cardiologic work-up revealed a left anterior hemiblock, mild myocardial thickening, and noncompaction. This case shows that myotilinopathy may manifest as a multisystem disease, including noncompaction. |
format | Online Article Text |
id | pubmed-7244945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-72449452020-06-05 Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T Finsterer, Josef Stöllberger, Claudia Hasun, Matthias Riedhammer, Korbinian Wagner, Mathias Case Rep Cardiol Case Report Left ventricular hypertrabeculation/noncompaction is a myocardial abnormality of unknown etiology/pathogenesis, which is frequently associated with neuromuscular disorders or chromosomal defects. LVHT in association with a MYOT mutation has not been reported. The patient is a 72-year-old male with a history of strabismus in childhood, asymptomatic creatine-kinase elevation since age 42 years, slowly progressive lower limb weakness since age 60 years, slowly progressive dysarthria and dysphagia since age 62 years, and recurrent episodes of arthralgias and myalgias since age 71 years. He also had arterial hypertension, diverticulosis, hyperlipidemia, coronary heart disease, and a hiatal hernia with reflux esophagitis. Clinical exam revealed mild quadruparesis and proximal wasting of the legs. Whole exome sequencing revealed a known variant in the MYOT gene. Muscle biopsy, previously assessed as inclusion body myopathy, was compatible with the genotype after revision. Cardiologic work-up revealed a left anterior hemiblock, mild myocardial thickening, and noncompaction. This case shows that myotilinopathy may manifest as a multisystem disease, including noncompaction. Hindawi 2020-05-13 /pmc/articles/PMC7244945/ /pubmed/32509353 http://dx.doi.org/10.1155/2020/5128069 Text en Copyright © 2020 Josef Finsterer et al. http://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 Finsterer, Josef Stöllberger, Claudia Hasun, Matthias Riedhammer, Korbinian Wagner, Mathias Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T |
title | Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T |
title_full | Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T |
title_fullStr | Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T |
title_full_unstemmed | Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T |
title_short | Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT Variant c.179C>T |
title_sort | multisystem myotilinopathy, including myopathy and left ventricular noncompaction, due to the myot variant c.179c>t |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244945/ https://www.ncbi.nlm.nih.gov/pubmed/32509353 http://dx.doi.org/10.1155/2020/5128069 |
work_keys_str_mv | AT finstererjosef multisystemmyotilinopathyincludingmyopathyandleftventricularnoncompactionduetothemyotvariantc179ct AT stollbergerclaudia multisystemmyotilinopathyincludingmyopathyandleftventricularnoncompactionduetothemyotvariantc179ct AT hasunmatthias multisystemmyotilinopathyincludingmyopathyandleftventricularnoncompactionduetothemyotvariantc179ct AT riedhammerkorbinian multisystemmyotilinopathyincludingmyopathyandleftventricularnoncompactionduetothemyotvariantc179ct AT wagnermathias multisystemmyotilinopathyincludingmyopathyandleftventricularnoncompactionduetothemyotvariantc179ct |