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Interstitial Deleti...
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Wentzel, ChristianUppsala universitet,Medicinsk genetik
(author)
Interstitial Deletions at 6q14.1-q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype
- Article/chapterEnglish2010
Publisher, publication year, extent ...
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2010-06-09
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S. Karger AG,2010
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printrdacarrier
Numbers
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LIBRIS-ID:oai:DiVA.org:uu-140215
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-140215URI
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https://doi.org/10.1159/000314025DOI
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https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-39240URI
Supplementary language notes
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Language:English
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Summary in:English
Part of subdatabase
Classification
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Notes
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BACKGROUNDInterstitial deletions of the long arm of chromosome 6 have been described in several patients with obesity and a Prader-Willi-like phenotype. Haploinsufficiency of the SIM1 gene located at 6q16.3 is suggested as being responsible for the regulation of body weight. Here we report on 2 patients with interstitial deletions at 6q14.1-q15 presenting with obesity and symptoms strikingly similar to those reported for deletions involving the SIM1 gene despite not having a deletion of this gene.METHODSArray comparative genomic hybridisation was used to diagnose 2 children with obesity and developmental delay, revealing 2 interstitial deletions at 6q14.1-q15 of 8.73 and 4.50 Mb, respectively, and a region of overlap of 4.2-Mb.RESULTSThe similar phenotype in the 2 patients was most likely due to a 4.2-Mb common microdeletion at 6q14.1-q15. Another patient has previously been described with an overlapping deletion. The 3 patients share several features, such as developmental delay, obesity, hernia, rounded face with full cheeks, epicanthal folds, short palpebral fissures, bulbous nose, large ears, and syndactyly between toes II and III.CONCLUSIONSTogether with a previously reported patient, our study suggests that the detected deletions may represent a novel clinically recognisable microdeletion syndrome caused by haploinsufficiency of dosage-sensitive genes in the 6q14.1-q15 region.
Subject headings and genre
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6q Deletion
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Learning disability
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Mental retardation
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Obesity
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MEDICINE
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MEDICIN
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Clinical genetics
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Klinisk genetik
Added entries (persons, corporate bodies, meetings, titles ...)
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Lynch, S. A.National Centre for Medical Genetics, OLCHC, Dublin, Ireland
(author)
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Stattin, Eva-LenaUmeå universitet,Medicinsk och klinisk genetik,Department of Medical Biosciences, Medical and Clinical Genetics, Umeå University, Umeå, Sweden(Swepub:umu)evst0015
(author)
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Sharkey, F. H.Microarray Unit, Cytogenetics Laboratory, Western General Hospital, Edinburgh, UK
(author)
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Annerén, GöranUppsala universitet,Medicinsk genetik(Swepub:uu)goraanne
(author)
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Thuresson, Ann-CharlotteUppsala universitet,Medicinsk genetik(Swepub:uu)anncthur
(author)
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Uppsala universitetMedicinsk genetik
(creator_code:org_t)
Related titles
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In:Molecular Syndromology: S. Karger AG1:2, s. 75-811661-87691661-8777
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