De novo 617G-A nucleotide mutation in the ACVR1 gene in a Taiwanese patient with fibrodysplasia ossificans progressiva

J Hum Genet. 2006;51(12):1083-1086. doi: 10.1007/s10038-006-0069-2. Epub 2006 Nov 1.

Abstract

Fibrodysplasia ossificans progressiva (FOP) is a rare congenital disease with autosomal dominant transmission characterized by the presence of malformations of the big toes and of postnatal progressive heterotopic endochondral osteogenesis. We report the case of 3-year-old girl with dysplasia of the first metatarsal bones and progressive heterotopic ossificans of the right thigh due to previous diphtheria-tetanus-pertussis immunizations and several inappropriate surgical interventions. Direct sequence analysis identified a 617G-A nucleotide mutation in the patient but not in her parents or brother. Pedigree analysis suggests that a de novo mutation in the ACVR1 gene is responsible for the disease in this family. This is the first report of the results of a mutation analysis in a sporadic case of FOP in a Taiwanese patient.

Publication types

  • Case Reports

MeSH terms

  • Activin Receptors, Type I / genetics*
  • Base Sequence
  • Child, Preschool
  • Female
  • Humans
  • Molecular Sequence Data
  • Myositis Ossificans / diagnosis
  • Myositis Ossificans / genetics*
  • Myositis Ossificans / pathology
  • Pedigree
  • Point Mutation*
  • Sequence Analysis, DNA
  • Taiwan

Substances

  • ACVR1 protein, human
  • Activin Receptors, Type I