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Chimerism 47, XY, +21/46, XX in a female infant with anencephaly and other congenital defects
Lucon, Danielle R; Zanchetta, Luciene M; Cavalcanti, Denise P.
  • Lucon, Danielle R; Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Genética Médica. Campinas. BR
  • Zanchetta, Luciene M; Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Genética Médica. Campinas. BR
  • Cavalcanti, Denise P; Universidade Estadual de Campinas. Faculdade de Ciências Médicas. Departamento de Genética Médica. Campinas. BR
Genet. mol. biol ; 29(1): 36-37, 2006. ilus
Article in English | LILACS | ID: lil-423416
ABSTRACT
Chimerism is rare in humans and is usually discovered accidentally when a 46,XX and 46,XY karyotype is found in a same individual. We describe a malformed female infant with neural tube defect (NTD) and a 47,XY,+21[5]/46,XX[30] karyotype.
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Full text: Available Index: LILACS (Americas) Main subject: Sex Chromosome Aberrations / Chimera Limits: Female / Humans / Infant, Newborn Language: English Journal: Genet. mol. biol Journal subject: Genetics Year: 2006 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual de Campinas/BR

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Full text: Available Index: LILACS (Americas) Main subject: Sex Chromosome Aberrations / Chimera Limits: Female / Humans / Infant, Newborn Language: English Journal: Genet. mol. biol Journal subject: Genetics Year: 2006 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual de Campinas/BR