Copyright
©The Author(s) 2022.
World J Clin Cases. Jul 16, 2022; 10(20): 7060-7067
Published online Jul 16, 2022. doi: 10.12998/wjcc.v10.i20.7060
Published online Jul 16, 2022. doi: 10.12998/wjcc.v10.i20.7060
Figure 1 The patient’s appearance, her pedigree and DNA analysis.
A: Bilateral facial & jaw muscle weakness of the patient; B: The pedigree of this family with myotonic dystrophy type 1; C: DNA analysis indicated that amplified cytosine-thymine-guanine trinucleotide repeated over 100 times present in the 3′ untranslated region of the DMPK gene of the proband (Ⅲ8), her mother (Ⅱ10), and her uncle (Ⅱ13).
- Citation: Jia YX, Dong CL, Xue JW, Duan XQ, Xu MY, Su XM, Li P. Myotonic dystrophy type 1 presenting with dyspnea: A case report. World J Clin Cases 2022; 10(20): 7060-7067
- URL: https://www.wjgnet.com/2307-8960/full/v10/i20/7060.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i20.7060