scholarly journals Sacral Neuromodulation in a Patient with Wolff-Parkinson-White Syndrome: A Case Report

2020 ◽  
Vol Volume 12 ◽  
pp. 193-197
Author(s):  
Sulaiman Almutairi
Keyword(s):  
Case Report ◽  
Sacral Neuromodulation ◽  
White Syndrome ◽  
Wolff Parkinson White Syndrome

scholarly journals Intervention in Undergoing Surgery with Undiagnosed Wolff-Parkinson-White Syndrome: Case Report

2020 ◽  
Vol 8 (3) ◽  
pp. 206-214
Author(s):  
Gezy Weita Giwangkancana ◽  
Astri Astuti ◽  
Dhany Budipratama ◽  
Aviryandi Wibawamukti ◽  
Fityan Aulia Rahman ◽  
...  
Keyword(s):  
Case Report ◽  
White Syndrome ◽  
Wolff Parkinson White Syndrome

scholarly journals A Case Report of Simultaneous Surgery for Wolff-Parkinson-White Syndrome Combined With Hemolytic Anemia and Mitral Stenosis

1996 ◽  
Vol 60 (3) ◽  
pp. 171-176 ◽  
Author(s):  
Masatoshi Ikeshita ◽  
Noboru Yamate ◽  
Shigeo Tanaka ◽  
Tetsuo Asano ◽  
Atsushi Harada ◽  
...  
Keyword(s):  
Case Report ◽  
Hemolytic Anemia ◽  
Mitral Stenosis ◽  
White Syndrome ◽  
Simultaneous Surgery ◽  
Wolff Parkinson White Syndrome

scholarly journals Case Report: m.13513 G>A Mutation in a Chinese Patient With Both Leigh Syndrome and Wolff-Parkinson-White Syndrome

2021 ◽  
Vol 9 ◽  
Author(s):  
Jian-Min Liang ◽  
Cui-Juan Xin ◽  
Guang-Liang Wang ◽  
Xue-Mei Wu
Keyword(s):  
Mitochondrial Dna ◽  
Case Report ◽  
Respiratory Failure ◽  
Developmental Delay ◽  
Nuclear Dna ◽  
Leigh Syndrome ◽  
Chinese Patient ◽  
White Syndrome ◽  
Wpw Syndrome ◽  
Wolff Parkinson White Syndrome

A number of causative mutations in mitochondrial and nuclear DNA have been identified for Leigh syndrome, a neurodegenerative encephalopathy, including m. 8993 T>G, m.8993 T>C, and m.3243A>G mutations in the MTATP6, MTATP6, and MT-TL1 genes, respectively, which have been reported in Leigh syndrome patients in China. The m.13513 G>A mutation has been described only a few times in the literature and not previously reported in China. Here we report the case of a 15-month-old boy who presented with ptosis and developmental delay and was diagnosed with Leigh syndrome and well as Wolff-Parkinson-White (WPW) syndrome. The m.13513 G>A mutation was found in DNA from blood. He was intubated due to respiratory failure and died at 23 months of age. The m.13513 G>A mutation in the ND5 gene of mitochondrial DNA is associated with Leigh syndrome and WPW syndrome; however, this is the first report of this mutation in a patient in China, highlighting the geographical and racial variability of Leigh syndrome.

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