Abstract
Two patients are described with trisomy 5p, resulting from the segregation through 3 generations of a t(4:5) (q33 p14) translocation. In the same family, 2 subjects are affected by the 'cri du chat' syndrome. The complex of malformations observed in the 2 trisomic patients is closely comparable to that reported in the few, previously described cases. However, the nonspecific character of these malformations makes trisomy 5p not yet clinically definable as a syndrome.
| Translated title of the contribution | Trisomy 5p |
|---|---|
| Original language | Italian |
| Pages (from-to) | 63-73 |
| Number of pages | 11 |
| Journal | Acta Medica Auxologica |
| Volume | 8 |
| Issue number | 1 |
| Publication status | Published - 1976 |
ASJC Scopus subject areas
- Medicine(all)