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The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements
Authors:Kathryn D. McGowan  Joseph J. Weiser  Juli Horwitz  Sue Ann Berend  Christopher McCaskill  V. Reid Sutton  Lisa G. Shaffer
Affiliation:1. Radiology Associates/Greystone, Providence, RI, USA;2. Genzyme Genetics, Santa Fe, NM, USA;3. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA
Abstract:
We report the finding of paternal isodisomy for chromosome 14 in a fetus found to have a der(14;14)(q10;q10) by amniocentesis. The pregnancy was complicated by severe polyhydramnios and elevated amniotic fluid alpha-fetoprotein (AFP). The infant showed features consistent with paternal uniparental disomy (UPD) including postnatal growth retardation, poor respiratory function, feeding difficulties, and evidence of hypertrophic cardiomyopathy. The present case, in addition to other reported cases of UPD involving balanced acrocentric rearrangements, supports testing for UPD in prenatally detected Robertsonian translocations and isochromosomes. Copyright © 2002 John Wiley & Sons, Ltd.
Keywords:uniparental disomy  paternal disomy  chromosome 14  Robertsonian translocation  isochromosome  isodisomy
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