An infant with chromosomally normal parents was found to have double aneuploidy and a reciprocal translocation between chromosomes number 6 and 10. This cooccurrence may represent a very rare coincidence or may indicate that primary nondisjunction and chromosome rearrangements may be more than coinc
✦ LIBER ✦
XYY chromosomal complement, proven by fluorescence, in a child with trisomy 21: 48,XYY,21+
✍ Scribed by Osztovics, Magda ;Iv�dy, Gyula ;B�hler, Erica M.
- Publisher
- Springer-Verlag
- Year
- 1971
- Weight
- 377 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0018-7348
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We report on an 8-year-old girl with minor anomalies consistent with 18q -syndrome and mild developmental delay. Initially cytogenetics showed a terminal deletion of chromosome 21 with mosaicism for a small ring chromosome 21 as the only apparent karyotypic abnormality: mos 45,XX, -21/46,XX, + r(21)