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Case Reports
. 2002;13(4):433-40.

Partial trisomy 20q in a newborn with dextrocardia

M C Addor  1 , C Castagne, J L Micheli, D F Schorderet
Affiliations
  • PMID: 12558114
Case Reports

Partial trisomy 20q in a newborn with dextrocardia

M C Addor et al. Genet Couns. 2002.

Abstract

A female newborn is reported with dextrocardia and a partial trisomy 20q, derived from a t(2;20) paternal translocation. The most discriminating findings of the condition include brachycephaly, bulging forehead, deep set eyes, short nose, large ears, dimpled chin, short neck and a heart defect. Previously reported patients with this rare chromosomal anomaly are reviewed.

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