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Pregled bibliografske jedinice broj: 1195247

Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series


Šenjug, Petar; Nikuševa Martić, Tamara; Šenjug Perica, Marija; Oroz, Maja; Horaček, Matija; Gotovac Jerčić, Kristina; Galešić, Krešimir; Galešić Ljubanović, Danica
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

Poveznice na cjeloviti tekst rada:

doi hrcak.srce.hr

Citiraj ovu publikaciju:

Šenjug, Petar; Nikuševa Martić, Tamara; Šenjug Perica, Marija; Oroz, Maja; Horaček, Matija; Gotovac Jerčić, Kristina; Galešić, Krešimir; Galešić Ljubanović, Danica
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)
Šenjug, P., Nikuševa Martić, T., Šenjug Perica, M., Oroz, M., Horaček, M., Gotovac Jerčić, K., Galešić, K. & Galešić Ljubanović, D. (2021) Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series. Croatian medical journal, 62 (3), 204-214 doi:10.3325/cmj.2021.62.20 4.
@article{article, author = {\v{S}enjug, Petar and Niku\v{s}eva Marti\'{c}, Tamara and \v{S}enjug Perica, Marija and Oroz, Maja and Hora\v{c}ek, Matija and Gotovac Jer\v{c}i\'{c}, Kristina and Gale\v{s}i\'{c}, Kre\v{s}imir and Gale\v{s}i\'{c} Ljubanovi\'{c}, Danica}, year = {2021}, pages = {204-214}, DOI = {10.3325/cmj.2021.62.20 4}, keywords = {Alport syndrome, COL4A4}, journal = {Croatian medical journal}, doi = {10.3325/cmj.2021.62.20 4}, volume = {62}, number = {3}, issn = {0353-9504}, title = {Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series}, keyword = {Alport syndrome, COL4A4} }
@article{article, author = {\v{S}enjug, Petar and Niku\v{s}eva Marti\'{c}, Tamara and \v{S}enjug Perica, Marija and Oroz, Maja and Hora\v{c}ek, Matija and Gotovac Jer\v{c}i\'{c}, Kristina and Gale\v{s}i\'{c}, Kre\v{s}imir and Gale\v{s}i\'{c} Ljubanovi\'{c}, Danica}, year = {2021}, pages = {204-214}, DOI = {10.3325/cmj.2021.62.20 4}, keywords = {Alport syndrome, COL4A4}, journal = {Croatian medical journal}, doi = {10.3325/cmj.2021.62.20 4}, volume = {62}, number = {3}, issn = {0353-9504}, title = {Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series}, keyword = {Alport syndrome, COL4A4} }

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


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