Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis

• Published in: American journal of medical genetics. Part A Vol. 127A; no. 2; pp. 144 - 148
• Main Authors: Guanciali-Franchi, Paolo, Calabrese, Giuseppe, Morizio, Elisena, Fantasia, Donatella, Colosimo, Alessia, Rinaldi, Maria M., Cristini, Luciano, Simonelli, Andrea, Lonardo, Fortunato, Turci, Alessandra, Zatterale, Adriana, Laganà, Carmelo, Stuppia, Liborio, Sabatino, Giuseppe, Palka, Giandomenico
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.06.2004
• Subjects: Chromosome Aberrations - classification; Cytogenetic Analysis; Female; Humans; In Situ Hybridization, Fluorescence - methods; Italy; marker chromosomes; Pregnancy; Prenatal Diagnosis; prenatal/postnatal diagnosis; spectral karyotyping; Spectral Karyotyping - methods; Italy
• ISSN: 1552-4825; 1552-4833
• DOI: 10.1002/ajmg.a.20691

Extra structurally abnormal chromosomes (ESACs) and cryptic rearrangements are often associated with mental retardation and phenotypic abnormalities. In some cases their characterisation, using standard cytogenetic techniques and fluorescence in situ hybridization (FISH), is difficult and time consuming, where a fast and accurate identification is essential, especially when such chromosomal aberrations are found in prenatal diagnosis. A recent molecular technique, spectral karyotyping (SKY), based on the spectral signature of 24 chromosome‐specific painting probes labelled with different combinations of five fluorochromes, allows the simultaneous visualisation of all human chromosomes in different colours. We used SKY analysis on 14 cases with rare ESACs or cryptic unbalanced rearrangements found at pre‐ or postnatal diagnosis. SKY analysis permitted the classification of chromosome rearrangements in all 14 cases analysed in combination with FISH analysis. © 2004 Wiley‐Liss, Inc.