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©The Author(s) 2022.
World J Clin Cases. Jan 21, 2022; 10(3): 1056-1066
Published online Jan 21, 2022. doi: 10.12998/wjcc.v10.i3.1056
Published online Jan 21, 2022. doi: 10.12998/wjcc.v10.i3.1056
Figure 5 Head magnetic resonance imaging of case 2 at 10 mo and at 2 years and 11 mo of age.
A: Flat pons.; B: Arachnoid cyst in the right temporal pole; C and D: Abnormal signal of periventricular white matter neuronal migration disorder in bilateral frontal lobes; E and F: An abnormal signal of periventricular white matter, which was absorbed and considerably improved compared to that seen in the previous magnetic resonance imaging.
- Citation: Wu WJ, Sun SZ, Li BG. Congenital muscular dystrophy caused by beta1,3-N-acetylgalactosaminyltransferase 2 gene mutation: Two case reports. World J Clin Cases 2022; 10(3): 1056-1066
- URL: https://www.wjgnet.com/2307-8960/full/v10/i3/1056.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i3.1056