Maternal origin of a unique extra chromosome, der(9)(pter-->q13::q13-->q12:) in a girl with typical trisomy 9p syndrome.

Abstract

We report on a girl with the typical trisomy 9p syndrome who had an additional E-sized metacentric chromosome. On the basis of GTG- and CBG-banding, her karyotype was considered to be 47,XX,+der(9)(pter-->q13::q13-->q12:) de novo. Results of a fluorescence in situ hybridization study using a chromosome 9-specific painting probe were compatible with this cytogenetic interpretation. Molecular analyses of six highly polymorphic dinucleotide repeat loci on the short arm and the proximal long arm of chromosome 9 demonstrated that the girl inherited one allele from her father and two identical or different alleles from the mother. We speculated that the extra chromosome may have resulted from either nondisjunction of chromosome 9 followed by a U-type exchange and a crossing-over between different sister chromatids during maternal meiosis I and subsequent breakage and malsegregation during meiosis II, or nondisjunction during meiosis II followed by isochromosome formation in one of the two maternal chromosomes 9 and subsequent breakage.

• Authors: M Teraoka, K Narahara, Y Yokoyama, S Ninomiya, S Mizuta, T Une, Y Seino
• Journal: American journal of medical genetics (Am J Med Genet) Vol. 102 Issue 1 Pg. 25-8 (Jul 22 2001) ISSN: 0148-7299 [Print] United States
• PMID: 11471168 (Publication Type: Case Reports, Journal Article)
• Copyright: Copyright 2001 Wiley-Liss, Inc.

Topics

• Alleles
• Child, Preschool
• Chromosome Mapping
• Chromosomes, Human, Pair 9 (genetics)
• Cytogenetic Analysis
• Family Health
• Female
• Humans
• In Situ Hybridization, Fluorescence
• Microsatellite Repeats (genetics)
• Polymorphism, Genetic
• Syndrome
• Trisomy