Erschienen in:
01.07.2012 | Genetics
Normal sperm in a 2;2 homologous male translocation carrier
verfasst von:
Carolina Almeida, Sofia Dória, Maria Moreira, Joel Pinto, Alberto Barros
Erschienen in:
Journal of Assisted Reproduction and Genetics
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Ausgabe 7/2012
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Abstract
Purpose
Carriers of balanced structural chromosomal abnormalities are phenotypically normal but are at high risk of infertility. Translocations usually occur between two non-homologous chromosomes. When occur between homologous chromosomes, an extremely rare event, generally involve acrocentric chromosomes. We present an infertile male referred for genetic analysis with a pure balanced homologous 2;2 translocation and normal sperm in the ejaculate.
Methods
Conventional cytogenetic and fluorescence in situ hybridization (FISH) were used in karyotype and sperm analysis, respectively.
Results
Male’s karyotype revealed a pure balanced translocation involving homologous chromosomes 2: 46,XY,t(2;2)(p23;q21.2). Sperm analysis by FISH revealed the presence of 15.8 % of normal and 84.2 % of abnormal spermatozoa for chromosome 2.
Conclusions
This is the first report of confined gonadal mosaicism in a pure homologous non-acrocentric chromosome translocation carrier. Preimplantation genetic diagnosis for chromosome 2 should be offered as a reproductive option.