Precocious puberty associated with partial trisomy 18q and monosomy 11q

Genet Couns. 2007;18(2):201-7.

Abstract

We report a 10-years-old female patient with a partial trisomy 18q and monosomy 11q due to a maternal translocation. The phenotype of our proband is partially common with Jacobsen syndrome and duplication 18q but she has also some atypical anomalies such as precocious puberty, a retinal albinism and hypermetropia. Based on cytogenetics and FISH analysis, the karyotype of the proband was 46,XX,der(11)t(11;18)(q24;q13). To the best of our knowledge, this is the first report of precocious puberty associated with either dup(18q) or del(11q) syndromes.

Publication types

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

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics*
  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 11 / genetics*
  • Chromosomes, Human, Pair 18 / genetics*
  • Craniofacial Abnormalities / diagnosis
  • Craniofacial Abnormalities / genetics*
  • Developmental Disabilities / diagnosis
  • Developmental Disabilities / genetics*
  • Facies
  • Female
  • Follow-Up Studies
  • Genetic Carrier Screening
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Monosomy / genetics*
  • Puberty, Precocious / genetics*
  • Translocation, Genetic / genetics
  • Trisomy / genetics*