Postnatal diagnosis of de novo complex der(8) in a boy with prenatal diagnosis of recombinant chromosome 8 syndrome.
Document Type
Article
Publication Date
5-1-2019
Abstract
Recombinant chromosome 8 syndrome is caused by duplication of 8q and deletion of 8p. A fetus with anomalies was misdiagnosed with this syndrome based on an amniocyte karyotype. Postnatal chromosomal microarray and other studies identified a de novo derivative chromosome 8. For fetal anomalies, detailed genetic studies may be required.
Publication Title
Clin Case Rep
ISSN
2050-0904
Volume
7
Issue
5
First Page
898
Last Page
902
Recommended Citation
Oren, Marina S; Jenny E Camacho; Hongyan Xie; Jean Lowe; Tom Cushing; Carol Clericuzio; and Jessie R Maxwell.
"Postnatal diagnosis of de novo complex der(8) in a boy with prenatal diagnosis of recombinant chromosome 8 syndrome.."
Clin Case Rep
COinS
