Article
Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case report.
Human reproduction (Oxford, England) - 1 Apr 2007
Malan Valérie, Gesny R, Morichon-Delvallez N, Aubry M C, Benachi A, Sanlaville D, Turleau C, Bonnefont J P, Fekete-Nihoul C, Vekemans M
Abstract excerpt
The phenotypic spectrum of 46,XX/46,XY chimeric patients is variable. It ranges from normal male or female genitalia to different degrees of ambiguous genitalia. Chimerism results from the amalgamation of two different zygotes in a single embryo, whereas mosaicism results from a mitotic error in a single zygote. Several other mechanisms resulting in a chimera have been discussed in the literature. Here, we report...
Topics
- Alleles
- Amniocentesis
- Chromosomes, Human, X
- Chromosomes, Human, Y
- Female
- Genotype
- Haploidy
- Humans
- Infant, Newborn
- Karyotyping
- Maternal Age
- Phenotype
- Polymorphism, Genetic
- Prenatal Diagnosis
