Prenatal Diagnosis of an Uncommon 48,XX,+18+21 Karyotype in a Fetus With Malformations Typical of Both Trisomies
J Ultrasound Med
.
2020 Nov;39(11):2277-2279.
doi: 10.1002/jum.15336.
Epub 2020 May 15.
Authors
Patrizia Fiorio
1
,
Gloria Donarini
2
,
Ezio Fulcheri
3
4
,
Gabriella Meccariello
2
,
Elisa Tassano
1
,
Giulia Amico
5
6
,
Dario Paladini
2
Affiliations
1
Human Genetics Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
2
Fetal Medicine and Surgery Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
3
Fetal and Perinatal Pathology Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
4
Division of Anatomic Pathology, Department of Surgical and Diagnostic Sciences, University of Genoa, Genoa, Italy.
5
Genetics and Genomics of Rare Diseases Unit, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Giannina Gaslini, Genoa, Italy.
6
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, and Maternal and Children's Sciences, University of Genoa, Genoa, Italy.
PMID:
32412111
DOI:
10.1002/jum.15336
No abstract available
Publication types
Letter
MeSH terms
Female
Fetus
Humans
Karyotype
Karyotyping
Pregnancy
Prenatal Diagnosis*
Trisomy* / diagnosis
Trisomy* / genetics