## Abstract Two syndromes with abnormalities of the short arm of chromosome 5 have been described: cri‐du‐chat (resulting from 5p deletion) and trisomy 5p. We report for the first time a patient with both syndromes, resulting from a complex chromosomal rearrangement with an inverted duplication of
De novo complex chromosomal rearrangement in a woman with recurrent spontaneous abortion and one healthy daughter
✍ Scribed by László Timár; Judit Béres; György Kosztolányi; Irén Németh
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 114 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0340-6717
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✦ Synopsis
Although rare, complex chromosomal rearrangements have been reported in the literature. The result is multiple congenital malformations in the offspring and recurrent spontaneous abortion. Chromosome 7 is usually involved, but in our patient chromosome 18 was involved.
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