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Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)
  1. BEATE ALBRECHT*,
  2. SUSANNE MERGENTHALER,
  3. KATJA EGGERMANN,
  4. KLAUS ZERRES,
  5. EBERHARD PASSARGE*,
  6. THOMAS EGGERMANN
  1. *Institute of Human Genetics, University of Essen, Germany
  2. †Institute of Human Genetics, Technical University of Aachen, Pauwelsstrasse 30, D-52074 Aachen, Germany
  1. Dr T Eggermann,teggermann{at}post.klinikum.rwth-aachen.de

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Editor—Recently, Bernasconiet al 1 and Shafferet al 2 described carriers of isochromosomes 2p (i(2p)) and 2q (i(2q)). In both patients maternal uniparental disomy (UPD) (2), the exceptional inheritance of both chromosomes 2 from the mother, was detected. Isochromosome formation of both the short and the long arms of a chromosome in one carrier is a rare event. In addition to isochromosomes 2, there exist single reports on only isochromosomes 4p and 4q,3 isochromosomes 7p and 7q,4 and isochromosomes 9p and 9q.5 In these cases, the parental origin was determined and was mostly maternal.

The phenotypes of the carriers of i(2p) and i(2q) and maternal UPD(2) are rather inconsistent. Bernasconi et al 1 reported a healthy woman with a history of five spontaneous abortions. In contrast, the patient of Shafferet al 2 showed features similar to those of three maternal UPD(2) patients ascertained because of confined placental mosaicism (CPM) for trisomy 2.6-8 In all these four patients, severe intrauterine growth retardation with …

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