[Gene diagnosis for spinal muscular atrophy and its application study]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):306-9. doi: 10.3760/cma.j.issn.1003-9406.2009.03.015.
[Article in Chinese]

Abstract

Objective: To establish an effective testing system for gene diagnosis, carrier detection and prenatal diagnosis for spinal muscular atrophy (SMA).

Methods: Twenty-six patients with SMA were directly tested with PCR-RFLP for exon 7 deletion in the SMN1 gene. Carrier detection was carried out with multi-PCR-DHPLC. Amniotic fluid was taken at the middle stage of gestation from pregnant women who had given birth to affected children.

Results: Twenty-five out of 26 patients were diagnosed as having SMN1 gene deletion. Fifty-two of their parents were found to be carriers of exon 7 deletion. Eight of 20 fetuses were diagnosed as having SMN1 gene deletion by PCR-RFLP.

Conclusion: PCR-RFLP and multi-PCR-DHPLC techniques can provide rapid diagnosis for exon 7 deletion detection and carrier detection. PCR-RFLP may also be adapted for prenatal gene diagnosis of exon 7 deletion in SMN1 gene.

Publication types

  • English Abstract

MeSH terms

  • Child
  • Exons / genetics*
  • Female
  • Gene Deletion*
  • Genetic Counseling
  • Humans
  • Male
  • Muscular Atrophy, Spinal / diagnosis*
  • Muscular Atrophy, Spinal / genetics
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Pregnancy
  • Prenatal Diagnosis
  • SMN Complex Proteins / genetics
  • Spinal Muscular Atrophies of Childhood / diagnosis*
  • Spinal Muscular Atrophies of Childhood / genetics
  • Survival of Motor Neuron 1 Protein / genetics*

Substances

  • SMN Complex Proteins
  • Survival of Motor Neuron 1 Protein