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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Junyang, Liu, Ming, Shang, Wenjie, Chen, Zhongqin, Peng, Guoping
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