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Am J Med Genet ; 113(3): 263-7, 2002 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-12439894

RESUMO

An 18-year-old woman was evaluated because of primary amenorrhea and hypogonadism. Chromosome analysis from peripheral blood lymphocytes revealed a nonmosaic 46,X,+mar constitution. The marker was shown to be a rearranged Y chromosome consisting of an inverted duplication of the long arm: rea(Y)(qter-q11::q11-qter). Deletion mapping analysis with Y-specific STS showed that the marker lacked Yp and Y-centromeric (DYZ3) sequences, but it was positive for Yq sequences tested. Fluorescence in situ hybridization analysis with Y and X chromosome centromeric and pancentromeric probes showed no hybridization signals. The marker chromosome is present in 100% of the cells; therefore, it is mitotically stable despite the absence of DYZ3 centromeric sequence. Hybridization with CENP-A and CENP-C specific antibodies localized a neocentromere close to the breakpoint.


Assuntos
Centrômero/genética , Cromossomos Humanos Y/genética , Aberrações dos Cromossomos Sexuais , Adolescente , Amenorreia/genética , Bandeamento Cromossômico , Feminino , Humanos , Hipogonadismo/genética , Hibridização in Situ Fluorescente , Proibitinas
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