Pregled bibliografske jedinice broj: 1195247
Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series
Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series // Croatian medical journal, 62 (2021), 3; 204-214 doi:10.3325/cmj.2021.62.20 4 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1195247 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Clinical and pathohistological characteristics of
Alport spectrum disorder caused by COL4A4 mutation
c.193-2A>C: a case series
Autori
Šenjug, Petar ; Nikuševa Martić, Tamara ; Šenjug Perica, Marija ; Oroz, Maja ; Horaček, Matija ; Gotovac Jerčić, Kristina ; Galešić, Krešimir ; Galešić Ljubanović, Danica
Izvornik
Croatian medical journal (0353-9504) 62
(2021), 3;
204-214
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Alport syndrome ; COL4A4
Sažetak
Aim: To present the pathohistological and clinical characteristics of five Croatian families with Alport spectrum disorders caused by splice acceptor pathogenic variant c.193-2A>C in COL4A4 at the genomic position chr2:227985866. Methods: The study enrolled five probands with kidney biopsy analysis and five family members. Mutation screening was performed with Illumina MiSeq platform. The pathogenic variant was confirmed with standard dye-terminator sequencing. Results: The only homozygous patient, aged two, had proteinuria and hematuria with preserved kidney function and no extrarenal manifestations. This patient had changes characteristic for Alport syndrome observed on electron microscopy of the kidney biopsy. In the heterozygous group, six patients had hematuria, four biopsied probands had proteinuria, and only one had moderately reduced kidney function. Heterozygous probands had variable kidney biopsy findings. Three patients had thin glomerular basement membrane nephropathy visible on electron microscopy and focal segmental glomerulosclerosis on light microscopy, two of them with focal lamellation on electron microscopy. One heterozygous patient had changes characteristic for Alport syndrome on electron microscopy without focal segmental glomerulosclerosis. Conclusion: The homozygous patient had hematuria and proteinuria with preserved kidney function. The heterozygous patients presented with reasonably mild clinical phenotype and variable pathohistological findings.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
--IP-2014-09-2151 - Genotip-fenotip korelacija u Alportovom sindromu i nefropatiji tankih glomerularnih bazalnim membrana (GPofASandTBMN) (Galešić-Ljubanović, Danica) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb,
Klinika za infektivne bolesti "Dr Fran Mihaljević",
Klinička bolnica "Dubrava",
Klinički bolnički centar Zagreb,
Dječja bolnica Srebrnjak
Profili:
Matija Horaček
(autor)
Krešimir Galešić
(autor)
Kristina Gotovac Jerčić
(autor)
Tamara Nikuševa Martić
(autor)
Maja Oroz
(autor)
Petar Šenjug
(autor)
Danica Galešić Ljubanović
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE