Literature DB >> 6588751

Cat-eye syndrome with unusual marker chromosome probably not chromosome 22.

W Rosenfeld, R S Verma, R C Jhaveri.   

Abstract

An unusual supernumerary chromosome with a single satellite on the long arm was found in a child with manifestations of the cat-eye syndrome including apparently low-set and malformed ears, preauricular tags, micrognathia, and imperforate anus. Although G-banding suggested that this extra material was chromosome 22, this was not confirmed by several other banding techniques. After examination of the parents' chromosomes, the nature and origin of this extra chromosome remains obscure. We conclude that patients previously diagnosed as having "partial trisomy 22" with incomplete cat-eye syndrome may have a different chromosome constitution when studied by various banding techniques.

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Year:  1984        PMID: 6588751     DOI: 10.1002/ajmg.1320180105

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


  3 in total

1.  Forty four probands with an additional "marker" chromosome.

Authors:  K E Buckton; G Spowart; M S Newton; H J Evans
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Molecular characterization of the marker chromosome associated with cat eye syndrome.

Authors:  A J Mears; A M Duncan; M L Budarf; B S Emanuel; B Sellinger; J Siegel-Bartelt; C R Greenberg; H E McDermid
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

3.  Cat-Eye Syndrome: A Report of Two Cases and Literature Review.

Authors:  Nélia S Gaspar; Gustavo Rocha; Ana Grangeia; Henrique C Soares
Journal:  Cureus       Date:  2022-06-25
  3 in total

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