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J Forensic Sci. 2016 May;61(3):687-91. doi: 10.1111/1556-4029.13027. Epub 2016 Jan 4.

Molecular Autopsy of Desmosomal Protein Plakophilin-2 in Sudden Unexplained Nocturnal Death Syndrome.

Author information

1
Department of Forensic Pathology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China.
2
Department of Forensic Sciences, Faculty of Forensic Sciences, Guangdong Justice Police Vocational College, Guangzhou, 510520, China.
3
Department of Cardiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510080, China.

Abstract

Plakophilin-2 (PKP2) variants could produce a phenotype of Brugada syndrome (BrS), which seems to be most likely the same allelic disorder as some sudden unexplained nocturnal death syndrome (SUNDS). All coding regions of PKP2 gene in 119 SUNDS victims were genetically screened using PCR and direct Sanger sequencing methods. Three novel mutations (p.Ala159Thr, p.Val200Val, and p.Gly265Glu), one novel rare polymorphism (p.Thr723Thr), and eight reported polymorphisms were identified. A compound mutation (p.Ala159Thr and p.Gly265Glu) and a rare polymorphism (p.Thr723Thr) were found in one SUNDS case with absence of the cardiomyopathic features. The detected compound mutation identified in this first investigation of PKP2 genetic phenotype in SUNDS is regarded as the plausible genetic cause of this SUNDS case. The rare incidence of PKP2 mutation in SUNDS (1%) supports the previous viewpoint that SUNDS is most likely an allelic disorder as BrS.

KEYWORDS:

Brugada syndrome; arrhythmogenic right ventricular cardiomyopathy; forensic pathology; forensic science; genetics; plakophilin-2; sodium current; sudden cardiac death; sudden unexplained nocturnal death syndrome

PMID:
27122407
DOI:
10.1111/1556-4029.13027
[Indexed for MEDLINE]

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