Metaphyseal chondrodysplasia McKusick type in a Chinese fetus, caused by novel compound heterozygosity 64T> A and 79G >T in RMRPgene

Prenat Diagn. 2006 Nov;26(11):1018-20. doi: 10.1002/pd.1547.

Abstract

We present the first confirmed case by molecular analysis of a metaphyseal chondrodysplasia, McKusick type, in a 22-week fetus. Two novel compound heterozygous mutations, 64T> A and 79G > T, were found in the highly conserved regions of the RMRP gene. Twenty-two heterozygous g.1018 T> C mutations, two homozygous g.1018 T> C mutations, two heterozygous insertion mutations g.799_g.800insC and one heterozygous insertion mutation g.849_g.850insT were found among 100 normal controls. Careful radiological examination of the fetus for skeletal dysplasia allowed definitive diagnosis, proper genetic counselling and future prenatal diagnosis.

Publication types

  • Case Reports

MeSH terms

  • Abortion, Eugenic
  • Adult
  • Endoribonucleases / genetics*
  • Female
  • Heterozygote
  • Humans
  • Mutation
  • Osteochondrodysplasias / genetics*
  • Pregnancy
  • Sequence Analysis, DNA

Substances

  • Endoribonucleases
  • mitochondrial RNA-processing endoribonuclease