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Revista Cubana de Obstetricia y Ginecología
versión impresa ISSN 0138-600X
Resumen
SORIANO-TORRES, Michel; MORALES RODRIGUEZ, Enny; ROJAS BETANCOURT, Iris y MENDEZ ROSADO, Luis Alberto. Variants of heterochromatin and euchromatin in cytogenetic prenatal diagnosis. Rev Cubana Obstet Ginecol [online]. 2014, vol.40, n.1, pp. 79-88. ISSN 0138-600X.
Some changes in chromosome morphology, which are detected in cytogenetic diagnostics, are not associated with clinical defects presenting a dilemma for the genetic counsellor, especially during prenatal diagnosis; this is the reason why a proper discrimination between innocuous variants and true anomalies is crucial to allow precise counselling. Polymorphisms of heterochromatin are identified usually by specific banding techniques and considered as Mendelian variations without a clinical significance. Likewise, it has been exposed in the literature the presence of variants in euchromatic regions that after a detailed analysis turns out to be of benign nature. Due to the current importance of this issue it is necessary to propose a protocol to follow in our laboratories every time a chromosome variant is detected while performing a prenatal analysis and supported by experienced specialist in our field. The goal of this work is to present a review of the literature about how a finding of a chromosome variant is handled and the suggestions given for a more proper management.
Palabras clave : cytogenetic prenatal diagnosis; heteromorphic variants; euchromatic variants; heteromorphism.