1976PubMedRequires access

Partial trisomy of chromosome 14: (+14q-).

Yeatman Gw, Riccardi Vm

Open publisher page 10 citations

Abstract

Partial trisomy 14 as a 47, + 14q- karyotype is compatible with life and this state is distinguished on cytogenetic, not clinical, grounds. Clinical features are nonspecific and these children are most obvious because of growth and mental retardation. This extends and broadens the indications for chromosome analysis. The significance of finding a +14q- karyotype must, however, be considered in the knowledge that ESA fragments have been associated with disorders that do not have a chromosome aberration pathogenesis. A balanced translocation should always be sought in parents of affected children. Finally, the proximal long arm of chromosome 14 apparently has at least 2 sites of relative fragility: 14q12 in vitro and 14q22 in vivo. Blood group analyses have been uninformative (2, 5).

About this research paper

What this paper is about

Partial trisomy 14 as a 47, + 14q- karyotype is compatible with life and this state is distinguished on cytogenetic, not clinical, grounds. Clinical features are nonspecific and these children are most obvious because of growth and mental retardation. This extends and broadens the indications for chromosome analysis. The significance of finding a +14q- karyotype must, however, be considered in the knowledge that ESA fragments have been associated with disorders that do not have a chromosome aberration pathogenesis. A balanced translocation should always be sought in parents of affected children. Finally, the proximal long arm of chromosome 14 apparently has at least 2 sites of relative fragility: 14q12 in vitro and 14q22 in vivo. Blood group analyses have been uninformative (2, 5).

Why it matters

OpenAlex reports 10 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Partial trisomy 14 as a 47, + 14q- karyotype is compatible with life and this state is distinguished on cytogenetic, not clinical, grounds. Clinical features are nonspecific and these children are most obvious because of growth and mental retardation. This extends and broadens the indications for chromosome analysis. The significance of finding a +14q- karyotype must, however, be considered in the knowledge that ESA fragments have been associated with disorders that do not have a chromosome aberration pathogenesis. A balanced translocation should always be sought in parents of affected children. Finally, the proximal long arm of chromosome 14 apparently has at least 2 sites of relative fragility: 14q12 in vitro and 14q22 in vivo. Blood group analyses have been uninformative (2, 5).

Key concepts: Karyotype, Chromosomal translocation, Chromosome analysis, Trisomy, Chromosome, Partial Trisomy, Biology, Genetics

Related papers

Back to paper searchBrowse research topicsOriginal source
Partial trisomy of chromosome 14: (+14q-). — Research Paper | ScholarLens