Prenatal detection of a fetus hemizygous for the fragile X-chromosome |
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Authors: | Angela Schmidt E. Passarge Eva Seemanová M. Macek |
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Affiliation: | (1) Institut für Humangenetik, Universitätsklinikum Essen, Hufelandstr. 55, D-4300 Essen 1, Federal Republic of Germany;(2) Genetické oddelenî Ustavu výzkumu vývoje ditete FDL University Karlovy, Praha |
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Abstract: | Summary A male fetus of a pregnancy known to be at risk for X-linked mental retardation with fragile site Xq27 was found to be affected by demonstrating the marker X-chromosome in five of 180 (2.8%) of metaphases derived from amniocytes cultured in medium 199. The results were confirmed in fetal lymphocytes (25 of 86 metaphases, i.e. 29%), and fetal fibroblasts (five of 100 metaphases when cultured in medium 199, and 14 of 100 after exposure to methotrexate for 43 h).This work was supported in part by a research grant from the Deutsche Forschungsgemeinschaft |
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