TRISOMIA 5P

Translated title of the contribution: Trisomy 5p

B. Dallapiccola, A. Calabro, A. Forabosco, G. Preto

Research output: Contribution to journalArticle

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.

Original languageItalian
Pages (from-to)63-73
Number of pages11
JournalActa Medica Auxologica
Volume8
Issue number1
Publication statusPublished - 1976

    Fingerprint

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Dallapiccola, B., Calabro, A., Forabosco, A., & Preto, G. (1976). TRISOMIA 5P. Acta Medica Auxologica, 8(1), 63-73.