Literature DB >> 10694690

Dicentric marker derived from chromosome 22 associated with mild clinical signs: a case report.

L Lohmann1, N Chelloug, B Rosales, C Guérin, S Lyonnet, P Jonveaux, B Simon-Bouy.   

Abstract

Amniocentesis performed after 24 weeks' gestation following ultrasonographic diagnosis of isolated unilateral hydronephrosis showed a de novo extra structurally abnormal chromosome in all cells examined. A combination of conventional and molecular cytogenetic techniques characterized the supernumerary marker as a dicentric and bisatellited marker derived from chromosome 22. At birth the infant presented hypoplasia of the right kidney, hearing loss on the left side and bilateral preauricular pits and skin tags. At three years, growth and neurological development were normal. Copyright 2000 John Wiley & Sons, Ltd.

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Year:  2000        PMID: 10694690

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  1 in total

1.  Genotype-phenotype correlation in 75 patients with small supernumerary marker chromosomes.

Authors:  Tingting Li; Haiquan Sang; Guoming Chu; Yuanyuan Zhang; Manlong Qi; Xiaoliang Liu; Wanting Cui; Yanyan Zhao
Journal:  Mol Cytogenet       Date:  2020-07-14       Impact factor: 2.009

  1 in total

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