Prenatal Detection of De Novo Inversion of Chromosome 9 with Duplicated Heterochromatic Region and Postnatal Follow-up

Overview

Journal Exp Mol Med

Specialties Biochemistry
Molecular Biology

Date 1999 Nov 7

PMID 10551261

Citations 3

Authors

J J Kim

H S Rhee

Y T Chung

S Y Park

S K Choi

Affiliations

Soon will be listed here.

Abstract

We report the first de novo case of a heterochromatic duplication on the long arm of the chromosome 9, which then was pericentrically inverted at p11q13. This condition was detected prenatally and carry to term. We then performed the follow up for over 1 year. So far, there seems to be no phenotypical abnormalities.

Citing Articles

Pericentric Inversion of Chromosome 9 in Twins With Cyclopia: A Rare Entity.

Lah N, Taib F, Zon E, Ismail E, Annuar A Cureus. 2023; 15(2):e34562.

PMID: 36743908 PMC: 9894573. DOI: 10.7759/cureus.34562.

A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator.

Stamou M, Ng S, Brand H, Wang H, Plummer L, Best L J Clin Endocrinol Metab. 2019; 105(3).

PMID: 31628846 PMC: 7112981. DOI: 10.1210/clinem/dgz011.

De novo pericentric inversion of chromosome 9 in congenital anomaly.

Jeong S, Kim B, Yu J Yonsei Med J. 2010; 51(5):775-80.

PMID: 20635455 PMC: 2908878. DOI: 10.3349/ymj.2010.51.5.775.