Prenatal diagnosis of spinal muscular atrophy type I (Werdnig- hoffmann) by DNA deletion analysis of cultivated amniocytes

Croat Med J. 1999 Sep;40(3):433-7.

Abstract

Aim: Presentation of a prenatally diagnosed case of Werdnig-Hoffmann disease, the most severe type of spinal muscular atrophy.

Methods: DNA obtained from cultivated amniocytes was analyzed for deletions in the survival motor neuron gene and neuronal apoptosis inhibitory protein gene.

Results: The fetus was diagnosed as an affected homozygote for deletions in exon 7 and exon 8 of the survival motor neuron gene. No deletions of exon 5 in the neuronal apoptosis inhibitory protein gene were found.

Conclusion: Direct DNA deletion analysis of the survival motor neuron gene and neuronal apoptosis inhibitory protein gene in affected families represents a highly reliable and fast method for prenatal diagnosis of Werdnig-Hoffmann disease.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amniocentesis*
  • Amnion / cytology
  • Cells, Cultured
  • Cyclic AMP Response Element-Binding Protein
  • DNA / analysis
  • DNA / genetics*
  • Exons / genetics
  • Female
  • Gene Deletion*
  • Homozygote
  • Humans
  • Nerve Tissue Proteins / genetics
  • Neuronal Apoptosis-Inhibitory Protein
  • Pregnancy
  • RNA-Binding Proteins
  • Reproducibility of Results
  • SMN Complex Proteins
  • Spinal Muscular Atrophies of Childhood / diagnosis*

Substances

  • Cyclic AMP Response Element-Binding Protein
  • NAIP protein, human
  • Nerve Tissue Proteins
  • Neuronal Apoptosis-Inhibitory Protein
  • RNA-Binding Proteins
  • SMN Complex Proteins
  • DNA