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Title:Specific behavioural phenotype and secondary cognitive decline as a result of an 8.6 Mb deletion of 2q32.2q33.1
Authors:ID Gregorič Kumperščak, Hojka (Author)
ID Krgović, Danijela (Author)
ID Kokalj-Vokač, Nadja (Author)
Files:.pdf Journal_of_International_Medical_Research_2016_Gregoric_Kumperscak,_Krgovic,_Vokac_Specific_behavioural_phenotype_and_secondary_cognitiv.pdf (411,05 KB)
MD5: 5925FD4D31058E3D7E29DD318F6916B9
PID: 20.500.12556/dkum/f1cb4ca2-3adc-41a9-8800-c5f0d64d04f3
 
URL http://journals.sagepub.com/doi/10.1177/0300060515595651
 
Language:English
Work type:Scientific work
Typology:1.01 - Original Scientific Article
Organization:MF - Faculty of Medicine
Abstract:Chromosomal abnormalities involving 2q32q33 deletions are very rare and present with a specific phenotype. This case report describes a 37-year-old female patient with 2q32q33 microdeletion syndrome presenting with the characteristic features, but with the addition of secondary cognitive decline. Molecular karyotyping was performed on the patient and her parents. It revealed an 8.6 megabase deletion with the proximal breakpoint in the chromosome band 2q32.2 and the distal breakpoint in 2q33.1. The deletion encompassed 22 known genes, including the GLS, MYO1B, TMEFF2, PGAP1 and SATB2 genes. The observed deletion was confirmed using a paralogue ratio test. This case report provides further evidence that the SATB2 gene, together with GLS, MYO1B, TMEFF2 and possibly PGAP1, is a crucial gene in 2q32q33 microdeletion syndrome. The SATB2 gene seems to be crucial for the behavioural problems noted in our case, but deletion of the GLS, MYO1B and TMEFF2 genes presumably contributed to the more complex behavioural characteristics observed. Our patient is also, to our knowledge, the only patient with 2q32q33 microdeletion syndrome with secondary cognitive decline.
Keywords:2q32q33 microdeletion syndrome, behavioural problems, secondary cognitive decline, developmental delay, SATB2 gene
Publication status:Published
Publication version:Version of Record
Year of publishing:2016
Number of pages:str. 395-402
Numbering:Letn. 44, št. 2
PID:20.500.12556/DKUM-66848 New window
ISSN:0300-0605
UDC:575
ISSN on article:0300-0605
COBISS.SI-ID:5609791 New window
DOI:10.1177/0300060515595651 New window
NUK URN:URN:SI:UM:DK:VMYOEGAH
Publication date in DKUM:13.07.2017
Views:1493
Downloads:536
Metadata:XML DC-XML DC-RDF
Categories:Misc.
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Record is a part of a journal

Title:Journal of International Medical Research
Shortened title:J. Int. Med. Res.
Publisher:Sage Publications
ISSN:0300-0605
COBISS.SI-ID:28593625 New window

Licences

License:CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:http://creativecommons.org/licenses/by-nc/4.0/
Description:A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.
Licensing start date:13.07.2017

Secondary language

Language:Slovenian
Keywords:mikrodelecijski sindrom 2q32q33, vedenjski problemi, mikrodelecija, sindrom, sekundarni upad kognitivnih sposobnosti, zaostanek v razvoju, gen SATB2


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