Title
Cytogenetic and molecular characterization of a partial trisomy 2p arising from inverted duplication of 2p with terminal deletion of 2pter
Date Issued
01 November 2009
Access level
metadata only access
Resource Type
journal article
Author(s)
Henderson S.
Uddin N.
Stewart E.
Iyer S.
Ratner I.M.
Matthews E.
Doolittle J.
Garcia R.
Valdez F.
Dallaire S.
Appleberry T.
Payne D.
Collins R.
UT Southwestern Medical Center
Publisher(s)
Wiley-Blackwell
Abstract
Partial trisomy 2p is typically associated with partial monosomy of another chromosomal segment and results from a balanced translocation in one of the parents. Inverted duplications with terminal deletions have been reported in an increasing number of chromosomes. Several cases initially interpreted as terminal duplications have instead been documented to represent inverted duplications with terminal deletions. Inv dup del(2p) has been reported in patients who manifest the clinical findings of trisomy 2p syndrome. Here we report on a 2-month-old girl with inv dup del(2p) and clinical manifestations that overlap those found commonly in partial 2p trisomy, as previously reported in the literature. Her clinical picture helps delineate the phenotype of 2p duplication disorders. © 2009 Wiley-Liss, Inc.
Start page
2507
End page
2512
Volume
149
Issue
11
Language
English
OCDE Knowledge area
Genética humana Pediatría
Scopus EID
2-s2.0-70449377361
PubMed ID
Source
American Journal of Medical Genetics, Part A
ISSN of the container
15524833
Sources of information: Directorio de Producción Científica Scopus