Chimerism 47,XY,+21/46,XX in a female infant with anencephaly and other congenital defects

AUTOR(ES)

Lucon, Danielle R., Zanchetta, Luciene M., Cavalcanti, Denise P.

FONTE

Genetics and Molecular Biology

DATA DE PUBLICAÇÃO

2006

RESUMO

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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