Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1.
ABSTRACT Native American myopathy (NAM) is an autosomal recessive congenital myopathy first reported in the Lumbee Indian people. Features of NAM include congenital weakness, cleft palate, ptosis, short stature, and susceptibility to malignant hyperthermia provoked by anesthesia.
We identified five individuals with NAM from the Lumbee population, and hypothesized that these affected individuals have disease alleles shared identical-by-descent inherited from common ancestry. To identify a NAM disease locus, homozygosity mapping methods were employed on a genomewide 10K single-nucleotide polymorphism (SNP) screen. To confirm regions of homozygosity identified in the SNP screen, microsatellite repeat markers were genotyped within those homozygous segments.
The SNP data demonstrated five regions of shared homozygosity in individuals with NAM. The additional genotyping data narrowed the region to one common segment of homozygosity spanning D12S398 to rs3842936 mapping to 12q13.13-14.1. Notably, loss of heterozygosity estimates from the SNP data also detected this same 12q region in the affected individuals.
This study reports the first gene mapping of Native American myopathy (NAM) using single-nucleotide polymorphism-based homozygosity mapping in only a few affected individuals from simplex families and identified a novel NAM locus. Identifying the genetic basis of NAM may suggest new genetic etiologies for other more common conditions such as congenital myopathy and malignant hyperthermia.
Conference Proceeding: Polymorphic ventricular tachycardia in a model of triggered cardiac activity[show abstract] [hide abstract]
ABSTRACT: It has been suggested that the cardiac arrhythmia known as torsades de pointes could be caused by competing foci of triggered activity. To examine this competitive triggering hypothesis, we used a model of ventricular action potential propagation to simulate two separate zones of heterogeneous myocardium under electrophysiologic conditions that have been correlated with the occurrence of torsades de pointes. We found that the two zones could trigger competitively, and that the corresponding electrogram morphology alternates as observed during episodes of torsades de pointes. These preliminary results are in accord with the competitive triggering hypothesisEngineering in Medicine and Biology Society, 1994. Engineering Advances: New Opportunities for Biomedical Engineers. Proceedings of the 16th Annual International Conference of the IEEE; 02/1994