Literature DB >> 11536270

Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15.

D J Abrams1, A R Aronoff, S Ann Berend, B B Roa, L G Shaffer, M R Geier.   

Abstract

We report the prenatal diagnosis of a fetus with a de novo Robertsonian translocation: 45,XY,der(15;15)(q10;q10). Although Robertsonian translocations are common chromosomal rearrangements, those involving homologous chromosomes are infrequent. Since chromosome 15 is imprinted, uniparental disomy (UPD) is a concern when chromosomal rearrangements involving chromosome 15 are identified. In the present case, UPD studies showed normal biparental inheritance. In contrast to the fact that most homologous acrocentric rearrangements are isochromosomes, these results indicate postzygotic formation of a Robertsonian translocation between biparentally inherited chromosomes 15. Copyright 2001 John Wiley & Sons, Ltd.

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Year:  2001        PMID: 11536270     DOI: 10.1002/pd.133

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  2 in total

Review 1.  Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing.

Authors:  Moh-Ying Yip
Journal:  Transl Pediatr       Date:  2014-04

2.  Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases.

Authors:  Emese Horváth; Zsuzsanna Horváth; Dóra Isaszegi; Gyurgyinka Gergev; Nikoletta Nagy; János Szabó; László Sztriha; Márta Széll; Emőke Endreffy
Journal:  Mol Cytogenet       Date:  2013-09-08       Impact factor: 2.009

  2 in total

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