دورية أكاديمية

Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review

التفاصيل البيبلوغرافية
العنوان: Myotonic dystrophy type 1 accompanied with normal pressure hydrocephalus: a case report and literature review
المؤلفون: Junyang Wang, Ming Liu, Wenjie Shang, Zhongqin Chen, Guoping Peng
المصدر: BMC Neurology, Vol 20, Iss 1, Pp 1-6 (2020)
بيانات النشر: BMC, 2020.
سنة النشر: 2020
المجموعة: LCC:Neurology. Diseases of the nervous system
مصطلحات موضوعية: Myotonic dystrophy (DM1), Normal pressure hydrocephalus (NPH), Genetic testing, Muscular dystrophy, Neurology. Diseases of the nervous system, RC346-429
الوصف: Abstract 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.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-2377
العلاقة: https://doaj.org/toc/1471-2377Test
DOI: 10.1186/s12883-020-01636-0
الوصول الحر: https://doaj.org/article/e1ba6a7e8dba402aa669760d8147325bTest
رقم الانضمام: edsdoj.1ba6a7e8dba402aa669760d8147325b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14712377
DOI:10.1186/s12883-020-01636-0