A male newborn with a ring 10 chromosome is described. The distal part of the long arm of chromosome 10, deleted during ring formation (10q25), is translocated to the short arm of chromosome 19.
Malformative syndrome with ring chromosome 13
β Scribed by J. P. Fryns; J. Deroover; H. Berghe; J. J. Cassiman; P. Goffaux; E. Lebas
- Book ID
- 104703962
- Publisher
- Springer
- Year
- 1974
- Tongue
- English
- Weight
- 348 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A 46,XY,r(10) karyotype was found in lymphocytes and skin fibroblasts cultured from a 8-month-old male showing multiple malformations and severe mental retardation. A comparison of the clinical features observed in cases in which a 10 ring was identified by means of banding techniques has been also
Two new cases of ring chromosome 15 are reported. A review of the nine cases described in the literature shows that ring chromosomes 15 are associated with a rather uniform phenotype characterized by slight to moderate mental retardation, marked pre- and postnatal growth failure, triangular face, an