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Naslov:Specific behavioural phenotype and secondary cognitive decline as a result of an 8.6 Mb deletion of 2q32.2q33.1
Avtorji:ID Gregorič Kumperščak, Hojka (Avtor)
ID Krgović, Danijela (Avtor)
ID Kokalj-Vokač, Nadja (Avtor)
Datoteke:.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
 
Jezik:Angleški jezik
Vrsta gradiva:Znanstveno delo
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Opis: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.
Ključne besede:2q32q33 microdeletion syndrome, behavioural problems, secondary cognitive decline, developmental delay, SATB2 gene
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2016
Št. strani:str. 395-402
Številčenje:Letn. 44, št. 2
PID:20.500.12556/DKUM-66848 Novo okno
ISSN:0300-0605
UDK:575
COBISS.SI-ID:5609791 Novo okno
DOI:10.1177/0300060515595651 Novo okno
ISSN pri članku:0300-0605
NUK URN:URN:SI:UM:DK:VMYOEGAH
Datum objave v DKUM:13.07.2017
Število ogledov:1496
Število prenosov:536
Metapodatki:XML DC-XML DC-RDF
Področja:Ostalo
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Skupna ocena:(0 glasov)
Vaša ocena:Ocenjevanje je dovoljeno samo prijavljenim uporabnikom.
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Gradivo je del revije

Naslov:Journal of International Medical Research
Skrajšan naslov:J. Int. Med. Res.
Založnik:Sage Publications
ISSN:0300-0605
COBISS.SI-ID:28593625 Novo okno

Licence

Licenca:CC BY-NC 4.0, Creative Commons Priznanje avtorstva-Nekomercialno 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc/4.0/deed.sl
Opis:Licenca Creative Commons, ki prepoveduje komercialno uporabo, vendar uporabniki ne rabijo upravljati materialnih avtorskih pravic na izpeljanih delih z enako licenco.
Začetek licenciranja:13.07.2017

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:mikrodelecijski sindrom 2q32q33, vedenjski problemi, mikrodelecija, sindrom, sekundarni upad kognitivnih sposobnosti, zaostanek v razvoju, gen SATB2


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