Trisomy 10 mosaicism and maternal uniparental disomy 10 in a liveborn infant with severe congenital malformations

✍ Scribed by Johanne M.D. Hahnemann; Marta Nir; M. Friberg; Ulla Engel; Merete Bugge

• Publisher: John Wiley and Sons
• Year: 2005
• Tongue: English
• Weight: 66 KB
• Volume: 138A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.30908

✦ Synopsis

Abstract

We report on a liveborn infant with trisomy 10 mosaicism combined with maternal uniparental heterodisomy for chromosome 10. The mosaicism 47,XY,+10/46,XY was found in five different tissues, including one blood sample, while cultured lymphocytes from two other blood samples showed a normal karyotype, 46,XY. DNA analysis with six PCR‐based microsatellite markers demonstrated the trisomic cell line to be a result of maternal meiotic nondisjunction, and revealed maternal uniparental heterodisomy in the diploid cell line, suggesting that the formation of the diploid cell line was due to trisomy rescue. The boy had severe growth retardation, major dysmorphism, and malformations, and died at 37 days. We reviewed the previous nine reports of infants and fetuses with trisomy 10 mosaicism reported in the literature. We suggest that a common clinical syndrome can be defined comprising skull, jaw and ear abnormalities, cleft lip/palate, malformations of eyes, heart and kidneys, deformity of hands and feet, and most often death neonatally or in early infancy. The cytogenetic findings in the present patient demonstrate the importance of karyotyping more than one tissue, and not only lymphocytes, when a chromosomal aberration is strongly suspected. © 2005 Wiley‐Liss, Inc.