Literature DB >> 7681252

Interstitial deletion of 8q13.3-->22.1 associated with craniosynostosis.

J S Fryburg1, W L Golden.   

Abstract

We report on a 3-year-old girl who has an interstitial deletion of chromosome 8q [46,XX,del(8)(q13.3q22.1)]. She has severe mental retardation and minor anomalies in addition to lambdoidal synostosis. This is the first report of craniosynostosis in association with this chromosomal deletion. The manifestations of our patient are compared to those of previously reported patients with similar deletions.

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Year:  1993        PMID: 7681252     DOI: 10.1002/ajmg.1320450524

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  Characterization of a 8q21.11 microdeletion syndrome associated with intellectual disability and a recognizable phenotype.

Authors:  María Palomares; Alicia Delicado; Elena Mansilla; María Luisa de Torres; Elena Vallespín; Luis Fernandez; Victor Martinez-Glez; Sixto García-Miñaur; Julián Nevado; Fernando Santos Simarro; Victor L Ruiz-Perez; Sally Ann Lynch; Freddie H Sharkey; Ann-Charlotte Thuresson; Göran Annerén; Elga F Belligni; María Luisa Martínez-Fernández; Eva Bermejo; Beata Nowakowska; Anna Kutkowska-Kazmierczak; Ewa Bocian; Ewa Obersztyn; María Luisa Martínez-Frías; Raoul C M Hennekam; Pablo Lapunzina
Journal:  Am J Hum Genet       Date:  2011-07-28       Impact factor: 11.025

2.  Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development.

Authors:  Litu Zhang; Zeynep Tümer; Kjeld Møllgård; Gotthold Barbi; Eva Rossier; Eske Bendsen; Rikke Steensbjerre Møller; Reinhard Ullmann; Jian He; Nickolas Papadopoulos; Niels Tommerup; Lars Allan Larsen
Journal:  Eur J Hum Genet       Date:  2009-01-28       Impact factor: 4.246

  2 in total

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