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Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
Liehr, T; Utine, G E; Trautmann, U; Rauch, A; Kuechler, A; Pietrzak, J; Pietracz, J; Bocian, E; Kosyakova, N; Mrasek, K; Boduroglu, K; Weise, A; Aktas, D.
Afiliação
  • Liehr T; Institute of Human Genetics and Anthropology, Jena, Germany. i8lith@mti.uni-jena.de
Cytogenet Genome Res ; 118(1): 31-7, 2007.
Article em En | MEDLINE | ID: mdl-17901697
ABSTRACT
Here we report on three new patients with neocentric small supernumerary marker chromosomes (sSMC) derived from chromosome 2, 13 and 15, respectively. The sSMC(13) and sSMC(15) had inverted duplicated shapes and the sSMC(2) a ring chromosome shape. All three cases were clinically severely abnormal. A review of the available sSMC literature revealed that up to the present 73 neocentric sSMC cases including these three new cases have been reported. Seven of these cases were not characterized morphologically; in the remainder, 80% had an inverted duplication, 17% a ring and 3% a minute shape. 81% of the reported neocentric sSMC carriers showed severe, 12% moderate and 8% no clinical abnormalities. In summary, we report three more neocentric sSMC cases, provide a review on all up to now published cases, highlight their special characteristics and compare them to centric sSMC.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 2 / Cromossomos Humanos Par 13 / Cromossomos Humanos Par 15 / Aberrações Cromossômicas Limite: Child / Female / Humans / Infant Idioma: En Revista: Cytogenet Genome Res Ano de publicação: 2007 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 2 / Cromossomos Humanos Par 13 / Cromossomos Humanos Par 15 / Aberrações Cromossômicas Limite: Child / Female / Humans / Infant Idioma: En Revista: Cytogenet Genome Res Ano de publicação: 2007 Tipo de documento: Article