[Spinal muscular atrophy carrier frequency in Ukraine]

Genetika. 2013 Sep;49(9):1126-8.
[Article in Russian]

Abstract

Background: Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder with the frequency of carriers in a number of ethnical groups ranging from 1/50 to 1/25. However, the prevalence of SMA for population of Ukraine remains to be established.

Methods: For the analysis of deletion in exon 7 SMN1 gene in SYBR Green Real-Time qPCR assay specific for the single nucleotide change in exon 7 (cd 840 C >T) was used.

Results: Using SYBR Green qPCR assay, the incidence of the exon 7 SMN1 deletion was established among 370 unrelated individuals without family history of SMA. The carrier frequency for this group of Ukrainians was estimated as 3.24% (1/31).

Conclusions: The results of our study showing the high prevalence of carriers warrant the importance of population screening for SMA in Ukraine.

Publication types

  • English Abstract

MeSH terms

  • Exons
  • Heterozygote*
  • Humans
  • Muscular Atrophy, Spinal / genetics*
  • Sequence Deletion
  • Survival of Motor Neuron 1 Protein / genetics*
  • Ukraine

Substances

  • SMN1 protein, human
  • Survival of Motor Neuron 1 Protein