Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study

J Med Genet. 1998 Nov;35(11):932-8. doi: 10.1136/jmg.35.11.932.

Abstract

We report on the characterisation of a complex chromosome rearrangement, 46,X,del(Xq)/47,X,del(Xq),+r(X), in a female newborn with multiple malformations. Cytogenetic and molecular methods showed that the del(Xq) contains the XIST locus and is non-randomly inactivated in all metaphases. The tiny r(X) chromosome gave a positive FISH signal with UBE1, ZXDA, and MSN cosmid probes, but not with a XIST cosmid probe. Moreover, it has an active status, as shown by a very short (three hour) terminal BrdU pulse followed by fluorescent anti-BrdU antibody staining. The normal X is of paternal origin and both rearranged chromosomes originate from the same maternal chromosome. We suggest that both abnormal chromosomes result from the three point breakage of a maternal isodicentric idic(X)(q21.1). Finally, the phenotype of our patient is compared to other published cases and, despite the absence of any 45,X clone, it appears very similar to those with a 45,X/46,X,r(X) karyotype where the tiny r(X) is active.

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Aberrations*
  • Chromosome Deletion
  • Dosage Compensation, Genetic
  • Female
  • Genomic Imprinting
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant, Newborn
  • Isochromosomes
  • Karyotyping
  • Male
  • Pedigree
  • Phenotype
  • RNA, Long Noncoding
  • RNA, Untranslated*
  • Ring Chromosomes*
  • Transcription Factors / genetics
  • X Chromosome*

Substances

  • RNA, Long Noncoding
  • RNA, Untranslated
  • Transcription Factors
  • XIST non-coding RNA