Literature DB >> 17710872

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

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


  2 in total

1.  Immune Deficiency in Jacobsen Syndrome: Molecular and Phenotypic Characterization.

Authors:  Raquel Rodríguez-López; Fátima Gimeno-Ferrer; Elena Montesinos; Irene Ferrer-Bolufer; Carola Guzmán Luján; David Albuquerque; Carolina Monzó Cataluña; Virginia Ballesteros; Monserrat Aleu Pérez-Gramunt
Journal:  Genes (Basel)       Date:  2021-07-31       Impact factor: 4.096

2.  Idiopathic central precocious puberty associated with 11 mb de novo distal deletion of the chromosome 9 short arm.

Authors:  Mariangela Cisternino; Erika Della Mina; Laura Losa; Alexandra Madè; Giulia Rossetti; Lorenzo Andrea Bassi; Giovanni Pieri; Baran Bayindir; Jole Messa; Orsetta Zuffardi; Roberto Ciccone
Journal:  Case Rep Genet       Date:  2013-07-31
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.