» Articles » PMID: 3804337

Prenatal Diagnosis of a 46,XX,inv(12)pat/47,XX,i(Xq),inv(12)pat

Overview
Journal Hum Genet
Specialty Genetics
Date 1987 Jan 1
PMID 3804337
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

A 46,XX,inv(12)pat/47,XX,i(Xq),inv(12)pat was diagnosed prenatally in a 36-year-old woman whose husband was a known carrier of a pericentric inversion of chromosome 12. The diagnosis was confirmed in fetal tissue. Terminal bromodeoxyuridine (BrdU) labelling demonstrated that in the line with 46 chromosomes one X was late replicating, while one X and the i(Xq) were late replicating in 100% of the cells with 47 chromosomes. We present the first case of this type of sex chromosome mosaicism. Genetic counseling presented difficulties since it was not possible to predict the fetal phenotype.

Citing Articles

Pericentric inversion of chromosome 12; a three family study.

Haagerup A, Hertz J Hum Genet. 1992; 89(3):292-4.

PMID: 1601419 DOI: 10.1007/BF00220542.

References
1.
Palmer C, Reichmann A . Chromosomal and clinical findings in 110 females with Turner syndrome. Hum Genet. 1976; 35(1):35-49. DOI: 10.1007/BF00295617. View

2.
Schmid W, Naef E, MURSET G, PRADER A . Cytogenetic findings in 89 cases of Turner's syndrome with abnormal karyotypes. Humangenetik. 1974; 24(2):93-104. DOI: 10.1007/BF00283766. View

3.
Fujita H, Tanigawa Y, Yoshida Y, Okada Y . Cytological findings of 10 cases with i(Xq) and one with dic(X)(qter leads to cen leads to p22::p11 leads to qter). Hum Genet. 1977; 39(2):147-55. DOI: 10.1007/BF00287006. View

4.
DAVIDENKOVA E, Verlinskaja D, Mashkova M . Structural aberrations of the X chromosome in man. Hum Genet. 1978; 41(3):269-79. DOI: 10.1007/BF00284761. View