Vaš brskalnik ne omogoča JavaScript!
JavaScript je nujen za pravilno delovanje teh spletnih strani. Omogočite JavaScript ali pa uporabite sodobnejši brskalnik.
Repozitorij Univerze v Ljubljani
Nacionalni portal odprte znanosti
Odprta znanost
DiKUL
slv
|
eng
Iskanje
Napredno
Novo v RUL
Kaj je RUL
V številkah
Pomoč
Prijava
Podrobno
Atypical COQ2-related retinopathy in identical twins with nephropathy mimicking intermediate uveitis
ID
Gavrič, Ana Uršula
(
Avtor
),
ID
Volk, Marija
(
Avtor
),
ID
Kojc, Nika
(
Avtor
),
ID
Osredkar, Damjan
(
Avtor
),
ID
Meglič, Andrej
(
Avtor
),
ID
Šuštar Habjan, Maja
(
Avtor
),
ID
Kiraly, Peter
(
Avtor
),
ID
Jaki Mekjavić, Polona
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(11,06 MB)
MD5: 0F62F9E4983BC7B29C0F061F4499DF35
URL - Izvorni URL, za dostop obiščite
https://www.tandfonline.com/doi/full/10.1080/09273948.2026.2679855
Galerija slik
Izvleček
Purpose: To describe an atypical presentation of COQ2-related retinopathy in identical twins withnephropathy, mimicking intermediate uveitis with cystoid macular oedema (CMO). Methods: Retrospective case report. Results: A 33-year-old man presented with bilateral vision worsening and suspected intermediate uveitis.Examination revealed vitreous cells, CMO, retinal microangiopathy, and severely abnormal electrooculo-graphy (EOG) with only borderline full-field electroretinography (ERG) changes. CMO worsened withtopical corticosteroids but improved bilaterally after a single unilateral intravitreal bevacizumab injection,suggesting a systemic therapeutic effect. His identical twin exhibited very similar retinal and systemicfindings. Whole-exome sequencing identified a homozygous likely pathogenic COQ2 variant (c.683A >G), confirming primary coenzyme Q10 (CoQ10) deficiency type 1. Both twins also had nephropathyconsistent with focal segmental glomerulosclerosis (FSGS) but no neurological involvement. Conclusions: This report expands the phenotypic spectrum of COQ2-related retinopathy, characterizedby retinal microangiopathy, CMO, and primary retinal pigment epithelium (RPE) dysfunction with pre-served rod function, in contrast to the typical retinitis pigmentosa–like phenotype. Recognition of thispresentation is critical, as early CoQ10 supplementation may stabilize disease progression and preventsystemic complications. Genetic testing should be considered in young patients with CMO resemblingintermediate uveitis, particularly when associated with nephropathy.
Jezik:
Angleški jezik
Ključne besede:
COQ2-related retinopathy
,
uveitis
,
rare disease
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2026
Št. strani:
Str. 1200-1205
Številčenje:
Vol. 34, iss.5
PID:
20.500.12556/RUL-185610
UDK:
617.7
ISSN pri članku:
1744-5078
DOI:
10.1080/09273948.2026.2679855
COBISS.SI-ID:
279820803
Datum objave v RUL:
13.08.2026
Število ogledov:
206
Število prenosov:
125
Metapodatki:
Citiraj gradivo
Navadno besedilo
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Kopiraj citat
Objavi na:
Gradivo je del revije
Naslov:
Ocular immunology and inflammation
Skrajšan naslov:
Ocul. immunol. inflamm.
Založnik:
Taylor & Francis
ISSN:
1744-5078
COBISS.SI-ID:
521279769
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Podobna dela
Podobna dela v RUL:
Podobna dela v drugih slovenskih zbirkah:
Nazaj