A family is reported with a segregating t(5;10)(p15;p11) translocation resulting in a child carrying trisomy 10p. The clinical findings of the patient are compared with trisomy 10p and the Cri-du-Chat syndrome.
Trisomy 10p due to a de novo t(10p;13p)
✍ Scribed by V. Aller; J. A. Abrisqueta; A. Pérez-Castillo; J. Mazo; M. A. Martín-Lucas; M. L. Torres
- Book ID
- 104707719
- Publisher
- Springer
- Year
- 1979
- Tongue
- English
- Weight
- 299 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0340-6717
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✦ Synopsis
A new case of trisomy 10p has been identified by means of the GTG-banding technique. The patient is a female child carrying a sporadic translocation, t(10;13)(p11;p11), and affected by microsomatia and microcephaly with facial dysmorphia, retarded growth, weight gain, and psychomotor development, and bilateral talipes.
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