[Translocation 11q;22q: a clinico-cytogenetic study].

Abstract

Seven families with translocations t(11; 22) identified at our Institute and analysis of the literature showed that the imbalance resulted from such translocations is always due to nondisjunction 3:1. Nondisjunction occurs more often in the 1st meiotic division, and is more rare in the second one. Expressed prezygotic selection against spermia with an additional chromosome greatly increases the risk of having an imbalanced child for the women-carriers as compared to men-carriers. The phenotype of the patients with +der(22)t(11; 22) is composed of the features characteristic for trisomy 22q (cleft lip and palate, preauricular papillomas and fistulas, rectal atresia or stenosis) and trisomy 11q (long philtrum with the upper lip hanging over, renal al; asia and hypoplasia). Diaphragmatic hernias are found to be common for the patients with +der(22)t(11; 22).

• Authors: I V Lur'e, N V Rumiantseva, L V Podleshchuk, S I Kozlova, V D Kulak, I V Naumchik, L B Gorelik, T V Zolotukhina, M I Kuznetsov
• Journal: Genetika (Genetika) Vol. 28 Issue 10 Pg. 129-35 (Oct 1992) ISSN: 0016-6758 [Print] Russia (Federation)
• Vernacular Title: Translokatsii 11q; 22q: kliniko-tsitogeneticheskoe issledovanie.
• PMID: 1468637 (Publication Type: Journal Article)

Topics

• Chromosomes, Human, Pair 11
• Chromosomes, Human, Pair 22
• Female
• Genetic Carrier Screening
• Humans
• Infant, Newborn
• Male
• Nondisjunction, Genetic
• Pregnancy
• Translocation, Genetic
• Trisomy