Multiple congenital abnormalities in a newborn with two supernumerary marker chromosomes derived from chromosome 14.
Publication year
2006Source
Genetic Counseling, 17, 3, (2006), pp. 349-57ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Journal title
Genetic Counseling
Volume
vol. 17
Issue
iss. 3
Page start
p. 349
Page end
p. 57
Subject
IGMD 3: Genomic disorders and inherited multi-system disorders; NCMLS 6: Genetics and epigenetic pathways of disease; UMCN 1.2: Molecular diagnosis, prognosis and monitoringAbstract
Pure partial duplication or triplication of the proximal part of chromosome 14 has been reported in only 4 patients. Other individuals with a duplication or triplication of this region have additional chromosome imbalances. We present a new case with a supernumerary marker chromosome in all blood cells and in 35% of the cells an additional smaller marker chromosome. Both markers appeared to be derived from chromosome 14 (del(14)(q21.2) in all cells and del(14)(q11.2) in 35% of the cells). This results in a partial duplication of the proximal region of chromosome 14, combined with a mosaic partial triplication of a smaller segment of the same region. In this paper, we compare the clinical features of this case to those of cases from the literature. Although most of the patients from literature were unbalanced translocation carriers, their clinical features were comparable, except from renal abnormalities.
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- Academic publications [232036]
- Faculty of Medical Sciences [89029]
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