Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10

<p>Abstract</p> <p>Background</p> <p>Genotype-phenotype correlations for chromosomal imbalances are often limited by overlapping effects of partial trisomy and monosomy resulting from unbalanced translocations and by poor resolution of banding analysis for breakpoint de...

Full description

Bibliographic Details
Main Authors: Weimer Jörg, Heidemann Simone, von Kaisenberg Constantin S, Grote Werner, Arnold Norbert, Bens Susanne, Caliebe Almuth
Format: Article
Language:English
Published: BMC 2011-12-01
Series:Molecular Cytogenetics
Subjects:
Online Access:http://www.molecularcytogenetics.org/content/4/1/28
id doaj-67a6600359cf4a6ca62317008757499d
record_format Article
spelling doaj-67a6600359cf4a6ca62317008757499d2020-11-25T01:58:31ZengBMCMolecular Cytogenetics1755-81662011-12-01412810.1186/1755-8166-4-28Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10Weimer JörgHeidemann Simonevon Kaisenberg Constantin SGrote WernerArnold NorbertBens SusanneCaliebe Almuth<p>Abstract</p> <p>Background</p> <p>Genotype-phenotype correlations for chromosomal imbalances are often limited by overlapping effects of partial trisomy and monosomy resulting from unbalanced translocations and by poor resolution of banding analysis for breakpoint designation. Here we report the clinical features of isolated partial trisomy 7q21.2 to 7q31.31 without overlapping phenotypic effects of partial monosomy in an 8 years old girl. The breakpoints of the unbalanced rearranged chromosome 7 could be defined precisely by array-CGH and a further imbalance could be excluded. The breakpoints of the balanced rearranged chromosomes 9 and 10 were identified by microdissection of fluorescence labelled derivative chromosomes 9 and 10.</p> <p>Results</p> <p>The proband's mother showed a complex balanced translocation t(9;10)(p13;q23) with insertion of 7q21.2-31.31 at the translocation breakpoint at 9p13. The daughter inherited the rearranged chromosomes 9 and 10 but the normal chromosome 7 from her mother, resulting in partial trisomy 7q21.2 to 7q31.31. The phenotype of the patient consisted of marked developmental retardation, facial dysmorphism, short stature, strabism, and hyperextensible metacarpophalangeal joints.</p> <p>Discussion</p> <p>For better understanding of genotype-phenotype correlation a new classification of 7q duplications which will be based on findings of molecular karyotyping is needed. Therefore, the description of well-defined patients is valuable. This case shows that FISH-microdissection is of great benefit for precise breakpoint designation in balanced rearrangements.</p> http://www.molecularcytogenetics.org/content/4/1/28chromosome microdissectionarray-CGHdevelopmental delayhypotoniaspeech-delayshort statureepicanthuspartial trisomy 7q21.2-7q31.31
collection DOAJ
language English
format Article
sources DOAJ
author Weimer Jörg
Heidemann Simone
von Kaisenberg Constantin S
Grote Werner
Arnold Norbert
Bens Susanne
Caliebe Almuth
spellingShingle Weimer Jörg
Heidemann Simone
von Kaisenberg Constantin S
Grote Werner
Arnold Norbert
Bens Susanne
Caliebe Almuth
Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
Molecular Cytogenetics
chromosome microdissection
array-CGH
developmental delay
hypotonia
speech-delay
short stature
epicanthus
partial trisomy 7q21.2-7q31.31
author_facet Weimer Jörg
Heidemann Simone
von Kaisenberg Constantin S
Grote Werner
Arnold Norbert
Bens Susanne
Caliebe Almuth
author_sort Weimer Jörg
title Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
title_short Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
title_full Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
title_fullStr Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
title_full_unstemmed Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
title_sort isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
publisher BMC
series Molecular Cytogenetics
issn 1755-8166
publishDate 2011-12-01
description <p>Abstract</p> <p>Background</p> <p>Genotype-phenotype correlations for chromosomal imbalances are often limited by overlapping effects of partial trisomy and monosomy resulting from unbalanced translocations and by poor resolution of banding analysis for breakpoint designation. Here we report the clinical features of isolated partial trisomy 7q21.2 to 7q31.31 without overlapping phenotypic effects of partial monosomy in an 8 years old girl. The breakpoints of the unbalanced rearranged chromosome 7 could be defined precisely by array-CGH and a further imbalance could be excluded. The breakpoints of the balanced rearranged chromosomes 9 and 10 were identified by microdissection of fluorescence labelled derivative chromosomes 9 and 10.</p> <p>Results</p> <p>The proband's mother showed a complex balanced translocation t(9;10)(p13;q23) with insertion of 7q21.2-31.31 at the translocation breakpoint at 9p13. The daughter inherited the rearranged chromosomes 9 and 10 but the normal chromosome 7 from her mother, resulting in partial trisomy 7q21.2 to 7q31.31. The phenotype of the patient consisted of marked developmental retardation, facial dysmorphism, short stature, strabism, and hyperextensible metacarpophalangeal joints.</p> <p>Discussion</p> <p>For better understanding of genotype-phenotype correlation a new classification of 7q duplications which will be based on findings of molecular karyotyping is needed. Therefore, the description of well-defined patients is valuable. This case shows that FISH-microdissection is of great benefit for precise breakpoint designation in balanced rearrangements.</p>
topic chromosome microdissection
array-CGH
developmental delay
hypotonia
speech-delay
short stature
epicanthus
partial trisomy 7q21.2-7q31.31
url http://www.molecularcytogenetics.org/content/4/1/28
work_keys_str_mv AT weimerjorg isolatedtrisomy7q2123131resultingfromacomplexfamilialrearrangementinvolvingchromosomes79and10
AT heidemannsimone isolatedtrisomy7q2123131resultingfromacomplexfamilialrearrangementinvolvingchromosomes79and10
AT vonkaisenbergconstantins isolatedtrisomy7q2123131resultingfromacomplexfamilialrearrangementinvolvingchromosomes79and10
AT grotewerner isolatedtrisomy7q2123131resultingfromacomplexfamilialrearrangementinvolvingchromosomes79and10
AT arnoldnorbert isolatedtrisomy7q2123131resultingfromacomplexfamilialrearrangementinvolvingchromosomes79and10
AT benssusanne isolatedtrisomy7q2123131resultingfromacomplexfamilialrearrangementinvolvingchromosomes79and10
AT caliebealmuth isolatedtrisomy7q2123131resultingfromacomplexfamilialrearrangementinvolvingchromosomes79and10
_version_ 1724969213396779008