| Literature DB >> 563312 |
B Dallapiccola, P P Mastroiacovo, E Montali, A Sommer.
Abstract
Five new cases of trisomy of the short arm of chromosome No. 4 are presented. In two brothers the abnormality arose from segregation of the 4p chromosome present in the mother who is a carrier of a centric fission of one No. 4 chromosome. In the other three patients, the chromosome imbalance originated from segregation of a balanced maternal 3p/4q or 4/22 translocation. The available data, derived from the 4p trisomics reported so far, are adequate to establish trisomy of the short arm of chromosome No. 4 as a definite clinical entity. The most outstanding findings include growth retardation of prenatal onset, severe mental deficiency, microcephaly and a peculiar constellation of facial dysmorphisms. The dermatoglyphic patterns and the radiological findings may help towards a correct interpretation of the syndrome.Entities:
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Year: 1977 PMID: 563312 DOI: 10.1111/j.1399-0004.1977.tb00953.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438