Cargando…
Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review
BACKGROUND: Myotonic dystrophy type 1 (DM1) is the most common disease that can cause muscle weakness and atrophy among adults. Normal pressure hydrocephalus (NPH) is characterized by the triad of gait disturbance, cognitive impairment and urinary incontinence. The association between DM1 and NPH is...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017494/ https://www.ncbi.nlm.nih.gov/pubmed/32050933 http://dx.doi.org/10.1186/s12883-020-01636-0 |
_version_ | 1783497205429043200 |
---|---|
author | Wang, Junyang Liu, Ming Shang, Wenjie Chen, Zhongqin Peng, Guoping |
author_facet | Wang, Junyang Liu, Ming Shang, Wenjie Chen, Zhongqin Peng, Guoping |
author_sort | Wang, Junyang |
collection | PubMed |
description | BACKGROUND: Myotonic dystrophy type 1 (DM1) is the most common disease that can cause muscle weakness and atrophy among adults. Normal pressure hydrocephalus (NPH) is characterized by the triad of gait disturbance, cognitive impairment and urinary incontinence. The association between DM1 and NPH is extremely rare. We report a Chinese female patient with DM1 in association with NPH. CASE PRESENTATION: The patient presented with a history of 3-year of walking instability and cognitive impairment. Her brain MRI showed ventriculomegaly with normal cerebrospinal fluid (CSF) pressure and the CSF tap-test was positive, which indicated the diagnosis of probable NPH. DM1 was confirmed by genetic testing. CONCLUSIONS: Four patients with DM1-NPH association were found before. The association between NPH and DM1 may not be just a coincidence, NPH may occur in DM1 later in life and it is vital to recognize the association as a shunt surgery may improve patients’ quality of life. |
format | Online Article Text |
id | pubmed-7017494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70174942020-02-20 Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review Wang, Junyang Liu, Ming Shang, Wenjie Chen, Zhongqin Peng, Guoping BMC Neurol Case Report BACKGROUND: Myotonic dystrophy type 1 (DM1) is the most common disease that can cause muscle weakness and atrophy among adults. Normal pressure hydrocephalus (NPH) is characterized by the triad of gait disturbance, cognitive impairment and urinary incontinence. The association between DM1 and NPH is extremely rare. We report a Chinese female patient with DM1 in association with NPH. CASE PRESENTATION: The patient presented with a history of 3-year of walking instability and cognitive impairment. Her brain MRI showed ventriculomegaly with normal cerebrospinal fluid (CSF) pressure and the CSF tap-test was positive, which indicated the diagnosis of probable NPH. DM1 was confirmed by genetic testing. CONCLUSIONS: Four patients with DM1-NPH association were found before. The association between NPH and DM1 may not be just a coincidence, NPH may occur in DM1 later in life and it is vital to recognize the association as a shunt surgery may improve patients’ quality of life. BioMed Central 2020-02-12 /pmc/articles/PMC7017494/ /pubmed/32050933 http://dx.doi.org/10.1186/s12883-020-01636-0 Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Wang, Junyang Liu, Ming Shang, Wenjie Chen, Zhongqin Peng, Guoping Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review |
title | Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review |
title_full | Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review |
title_fullStr | Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review |
title_full_unstemmed | Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review |
title_short | Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review |
title_sort | myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017494/ https://www.ncbi.nlm.nih.gov/pubmed/32050933 http://dx.doi.org/10.1186/s12883-020-01636-0 |
work_keys_str_mv | AT wangjunyang myotonicdystrophytype1accompaniedwithnormalpressurehydrocephalusacasereportandliteraturereview AT liuming myotonicdystrophytype1accompaniedwithnormalpressurehydrocephalusacasereportandliteraturereview AT shangwenjie myotonicdystrophytype1accompaniedwithnormalpressurehydrocephalusacasereportandliteraturereview AT chenzhongqin myotonicdystrophytype1accompaniedwithnormalpressurehydrocephalusacasereportandliteraturereview AT pengguoping myotonicdystrophytype1accompaniedwithnormalpressurehydrocephalusacasereportandliteraturereview |