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Overlapping phenoty...
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Mikhail, Fady M.
(author)
Overlapping phenotype of wolf-hirschhorn and beckwith-wiedemann syndromes in a girl with der(4)t(4; 1 1)(pter;pter)
- Article/chapterEnglish2007
Publisher, publication year, extent ...
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2007
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Wiley,2007
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printrdacarrier
Numbers
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LIBRIS-ID:oai:DiVA.org:uu-13613
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-13613URI
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https://doi.org/10.1002/ajmg.a.31821DOI
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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We report on an 8-month-old girl with a novel unbalanced chromosomal rearrangement, consisting of a terminal deletion of 4p and a paternal duplication of terminal 11p. Each of these is associated with the well-known clinical phenotypes of Wolf-Hirschhorn syndrome (WHS) and Beckwith-Wiedemann syndrome (BWS), respectively. She presented for clinical evaluation of dysmorphic facial features, developmental delay, atrial septal defect (ASD), and left hydro-nephrosis. High-resolution cytogenetic analysis revealed a normal female karyotype, but subtelomeric fluorescence in situ hybridization (FISH) analysis revealed a der(4)t(4;11) (pter;pter). Both FISH and microarray CGH studies clearly demonstrated that the WHS critical regions 1 and 2 were deleted, and that the BWS imprinted domains (ID) 1 and 2 were duplicated on the der(4). Parental chromosome analysis revealed that the father carried a cryptic balanced t(4;11)(pter;pter). As expected, our patient manifests findings of both WHS (a growth retardation syndrome) and BWS (an overgrowth syndrome). We compare her unique phenotypic features with those that have been reported for both syndromes.
Subject headings and genre
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Wolf-Hirschhorn syndrome (WHS)
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Beckwith-Wiedemann syndrome (BWS)
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fluorescence in situ hybridization (FISH)
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array CGH
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unbalanced translocation
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4p
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11p
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MEDICINE
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MEDICIN
Added entries (persons, corporate bodies, meetings, titles ...)
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Sathienkijkanchai, Achara
(author)
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Robin, Nathaniel H.
(author)
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Prucka, Sandra
(author)
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Biggerstaff, Julie Sanford
(author)
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Komorowski, JanUppsala universitet,Centrum för bioinformatik(Swepub:uu)jakom133
(author)
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Andersson, RobinUppsala universitet,Centrum för bioinformatik(Swepub:uu)roand427
(author)
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Bruder, CarlUppsala universitet,Institutionen för genetik och patologi
(author)
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Piotrowski, ArkadiuszUppsala universitet,Institutionen för genetik och patologi
(author)
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de Ståhl, Teresita DiazUppsala universitet,Institutionen för genetik och patologi(Swepub:uu)terstahl
(author)
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Dumanski, Jan P.Uppsala universitet,Institutionen för genetik och patologi(Swepub:uu)janduman
(author)
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Carroll, Andrew J.
(author)
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Uppsala universitetCentrum för bioinformatik
(creator_code:org_t)
Related titles
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In:American Journal of Medical Genetics, Part A: Wiley143:15, s. 1760-17661552-48251552-4833
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Prucka, Sandra
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Andersson, Robin
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