Literature DB >> 1785643

Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome.

M Clementi1, R Tenconi, L Turolla, C Silvan, L Bortotto, L Artifoni.   

Abstract

This report concerns 2 unrelated patients with apparent CHARGE association and a chromosome abnormality, resulting from different unbalanced familial translocations involving chromosomes 2 and 18 in one family, and chromosomes 3 and 22 in the other. Although the identification of two different chromosome abnormalities might be due to chance, the observation of a long arm deletion of chromosome 22 in patients 2 and of the frequent coexistence of CHARGE association and DiGeorge anomaly raise the possibility of a contiguous gene syndrome in at least some CHARGE cases.

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Year:  1991        PMID: 1785643     DOI: 10.1002/ajmg.1320410223

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


  7 in total

1.  Unilateral semicircular canal aplasia in Goldenhar's syndrome.

Authors:  M M Lemmerling; B D Vanzieleghem; G R Mortier; I J Dhooge; M F Kunnen
Journal:  AJNR Am J Neuroradiol       Date:  2000-08       Impact factor: 3.825

2.  CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.

Authors:  M C J Jongmans; R J Admiraal; K P van der Donk; L E L M Vissers; A F Baas; L Kapusta; J M van Hagen; D Donnai; T J de Ravel; J A Veltman; A Geurts van Kessel; B B A De Vries; H G Brunner; L H Hoefsloot; C M A van Ravenswaaij
Journal:  J Med Genet       Date:  2005-09-09       Impact factor: 6.318

Review 3.  Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome.

Authors:  Gabriel E Zentner; Wanda S Layman; Donna M Martin; Peter C Scacheri
Journal:  Am J Med Genet A       Date:  2010-03       Impact factor: 2.802

4.  Immune deficiency in CHARGE association.

Authors:  Demetrios S Theodoropoulos
Journal:  Clin Med Res       Date:  2003-01

5.  Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.

Authors:  Seema R Lalani; Arsalan M Safiullah; Susan D Fernbach; Karine G Harutyunyan; Christina Thaller; Leif E Peterson; John D McPherson; Richard A Gibbs; Lisa D White; Margaret Hefner; Sandra L H Davenport; John M Graham; Carlos A Bacino; Nancy L Glass; Jeffrey A Towbin; William J Craigen; Steven R Neish; Angela E Lin; John W Belmont
Journal:  Am J Hum Genet       Date:  2005-12-29       Impact factor: 11.025

6.  Features of DiGeorge syndrome and CHARGE association in five patients.

Authors:  P de Lonlay-Debeney; V Cormier-Daire; J Amiel; V Abadie; S Odent; A Paupe; S Couderc; A L Tellier; D Bonnet; M Prieur; M Vekemans; A Munnich; S Lyonnet
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

Review 7.  Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature.

Authors:  S Demczuk; A Lévy; M Aubry; M F Croquette; N Philip; M Prieur; U Sauer; P Bouvagnet; G A Rouleau; G Thomas
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

  7 in total

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