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Origin of chromosomal abnormalities: Evidence for delayed fertilization in meiotic nondisjunction

✍ Scribed by R. C. Juberg


Publisher
Springer
Year
1983
Tongue
English
Weight
500 KB
Volume
64
Category
Article
ISSN
0340-6717

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✦ Synopsis


This study ascertained 35 aneuploid patients, of which 34 had trisomy 21 and one had trisomy 18. Their parents were matched by age at the conception with parents of 35 euploid patients with congenital defects. Interviews with the couples focused on exposures and activities at the time of the conception. No parents had infectious hepatitis preceding the conception, and one study mother and four comparison parents reported drug ingestion. Eight parents in the study group and two in the comparison reported radiation exposure. One family in each group had a history of thyroid disorder. The groups differed mainly in their sexual histories; circumstances favoring the possibility of delayed fertilization (contraceptive failure, infrequency of intercourse, or premarital conception) existed in 22 of the study group but in only seven of the comparison group.


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The origin of trisomy 22: Evidence for a
✍ Heather E. Hall; Urvashi Surti; Lori Hoffner; Sofia Shirley; Eleanor Feingold; T πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 131 KB

## Abstract Trisomy 22 is one of the most common trisomies in clinically recognized pregnancies, yet relatively little is known about the origin of nondisjunction for chromosome 22. Accordingly, we initiated studies to investigate the origin of the extra chromosome in 130 trisomy 22 cases. Our resu