Literature DB >> 11208374

Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.

S L Cappon1, A M Duncan, M M Khalifa.   

Abstract

We report on a 28 year-old male with peculiar facies, distal joint contractures and other multiple congenital anomalies. Cytogenetic analysis by G banding revealed a distal tandem interstitial duplication of the long arm of chromosome q6, dup.(6)(6q24.2-->q26). This chromosome abnormality was confirmed by fluorescence in situ hybridization with total chromosome 6 painting. This is probably the second documented case of 6q duplication without growth retardation or severe psychomotor retardation. The clinical findings in our patient are similar to that of whistling face syndrome (WFS) and, in fact, he was diagnosed with WFS as a child. The literature were reviewed and the phenotypic features of this patient were compared with those previously reported for both duplication 6q and whistling face syndromes. There is a significant overlap between the phenotypes of these two syndromes. Careful evaluation of the terminal end of the 6q in cases suggestive of WFS might be warranted.

Entities:  

Mesh:

Year:  2000        PMID: 11208374

Source DB:  PubMed          Journal:  Med Sci Monit        ISSN: 1234-1010


  3 in total

1.  Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis.

Authors:  Anne-Claude Tabet; Azzedine Aboura; Marion Gérard; Marion Pilorge; Céline Dupont; Jean-François Gadisseux; Nadège Hervy; Eva Pipiras; Andrée Delahaye; Samia Kanafani; Alain Verloes; Brigitte Benzacken; Catalina Betancur
Journal:  Am J Med Genet A       Date:  2010-07       Impact factor: 2.802

2.  De Novo Subtelomeric 6p25.3 Deletion with Duplication of 6q23.3-q27: Genotype-Phenotype Correlation.

Authors:  Emine Ikbal Atli; Hakan Gurkan; Engin Atli; Ulfet Vatansever; Betul Acunas; Cisem Mail
Journal:  J Pediatr Genet       Date:  2019-08-12

3.  Interstitial 6q21q23 duplication - variant of variable phenotype and incomplete penetrance or benign duplication?

Authors:  Malgorzata I Srebniak; Laura J C M van Zutven; Florence Petit; Sonia Bouquillon; Ilse P J van Heel; Maarten F C M Knapen; Jerome M J Cornette; Andreas Kremer; Diane Van Opstal; Karin E M Diderich
Journal:  Mol Cytogenet       Date:  2016-06-02       Impact factor: 2.009

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.