| Literature DB >> 17710872 |
L Mutesa1, A C Hellin, M Jamar, G Pierquin, V Bours, A Verloes.
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.Entities:
Mesh:
Year: 2007 PMID: 17710872
Source DB: PubMed Journal: Genet Couns ISSN: 1015-8146