Pathological Findings in the Complete Trisomy 9 Syndrome: Three Case Reports and Review of the Literature

Author:

Ferreres Joan C.1,Planas Sílvia1,Martínez-Sáez Elena A.1,Vendrell Teresa1,Peg Vicente1,Salcedo M. Teresa1,Cajal Santiago Ramón Y1,Torán Núria1

Affiliation:

1. Department of Pathology and Genetics Unit, Hospital Universitari Vall d’ Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain

Abstract

The term “complete trisomy 9” is used to indicate trisomy of the entire chromosome 9 without evidence of mosaicisms. It is a relatively rare chromosomal abnormality because the vast majority of affected pregnancies result in 1st trimester spontaneous abortions. The purpose of this paper is to delineate the complete trisomy 9 syndrome, based on autopsy findings. We performed an exhaustive review of the literature of complete forms of this trisomy with autopsy examination and added 3 new cases from our center with new findings not previously described.

Publisher

SAGE Publications

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

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