Volume 39, Issue 2 pp. 151-155
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Ring chromosome 4 in a child with mild dysmorphic signs

Gabriele Freyberger

Gabriele Freyberger

Department of Human Genetics, University of Wuerzburg, Federal Republic of Germany

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Christine Wamsler

Christine Wamsler

Department of Human Genetics, University of Wuerzburg, Federal Republic of Germany

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Michael Schmid

Corresponding Author

Michael Schmid

Department of Human Genetics, University of Wuerzburg, Federal Republic of Germany

Department of Human Genetics University of Wuerzburg Koellikerstr. 2 D-8700 Wuerzburg Federal Republic of GermanySearch for more papers by this author
First published: February 1991
Citations: 11

Abstract

We report on an 8-year-old boy exhibiting microcephaly, clinodactyly and growth retardation. Chromosome analysis showed a ring chromosome 4 in 97% of the cells and a high number of hyperploid cells with various ring formations. The breakpoints are presumed to be close to or in the telomeric regions of both arms. The patients reported with ring chromosome 4 and breakpoints close to the telomeres of both arms showed unspecific, mild clinical findings with normal or retarded mental development. These signs are probably related to the continuous generation of aneuploid cells.

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