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Hum Genet. 1990 Jan;84(2):159-62.

Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36).

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  • 1Departamento de Biologia Celular y Fisiologia, Facultad de Medicina, Universidad Autónoma de Barcelona, Spain.


Meiotic and sperm chromosomes were studied in a man heterozygous for a reciprocal translocation t(1;2)(q32;q36). Forty-five meiotic metaphase I cells were obtained from semen samples: 86.6% were 22,XY,IV and 13.3% had synaptic anomalies that affected all or some of the bivalents. The quadrivalents observed had a ring configuration (92.3%) or a chain configuration (7.7%). A total of 105 sperm chromosome complements were analyzed: 41% resulted from an alternate segregation, and the percentage of unbalanced sperm was 59%; most of them (71%) resulted from an adjacent 1 segregation. The frequency of anomalies unrelated to the translocation (5.7% numerical and 14.1% structural anomalies) were within the normal range for control donors. There was a good correspondence between the percentage of cells with a ring IV (92.3%) and the proportion of 2:2 segregations (88.6%) and between the percentage of chain IV (7.7%) and the incidence of 3:1 segregations (11.4%).

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