Trisomy 13 by robertsonian translocation rob (13;13)(q10;q10) +13: about one case

Antoine Laudat; Stéphane Serero; Isma Seridi; Laurence Burc-Struxiano

doi:10.1684/abc.2017.1296

Trisomy 13 by robertsonian translocation rob (13;13)(q10;q10) +13: about one case

Ann Biol Clin (Paris). 2017 Dec 1;75(6):695-698. doi: 10.1684/abc.2017.1296.

Authors

Antoine Laudat¹, Stéphane Serero², Isma Seridi³, Laurence Burc-Struxiano¹

Affiliations

¹ Service de biologie médicale, Hôpital Louis Pasteur, Le Coudray, France.
² Centre de biologie et de cytogénétique médicales, Evreux, France.
³ Service de gynécologie-obstétrique, Hôpital Louis Pasteur, Le Coudray, France.

PMID: 29043983
DOI: 10.1684/abc.2017.1296

Abstract

We are reporting a rare case of foetal trisomy 13 due to a robertsnonian translocation. Further to the study of both parents karyotypes, genetic councelling is advisable in order to assess the potential risk of trisomy that may occur during a future pregnancy.

Keywords: case report; trisomy 13.

Publication types

Case Reports

MeSH terms

Abortion, Eugenic
Adult
Chromosomes, Human, Pair 13*
Female
Humans
Pregnancy
Prenatal Diagnosis
Translocation, Genetic*
Trisomy 13 Syndrome / diagnosis*
Trisomy 13 Syndrome / genetics
Trisomy 13 Syndrome / therapy