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Pregled bibliografske jedinice broj: 998380

The heart in Fabry’s disease


Skorup, Lea; Grgić Romić, Ivana; Šimić, Jelena; Vujičić, Božidar; Rački, Sanjin; Ružić, Alen; Zaputović, Luka; Matana, Ante; Zaninović Jurjević, Teodora
The heart in Fabry’s disease // Cardiologia Croatica 2019 ; 14(3-4)
Zagreb: Hrvatsko kardiološko društvo, 2019. str. 64-64 doi:10.15836/ccar2019.64 (poster, domaća recenzija, prošireni sažetak, stručni)


CROSBI ID: 998380 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
The heart in Fabry’s disease

Autori
Skorup, Lea ; Grgić Romić, Ivana ; Šimić, Jelena ; Vujičić, Božidar ; Rački, Sanjin ; Ružić, Alen ; Zaputović, Luka ; Matana, Ante ; Zaninović Jurjević, Teodora

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, prošireni sažetak, stručni

Izvornik
Cardiologia Croatica 2019 ; 14(3-4) / - Zagreb : Hrvatsko kardiološko društvo, 2019, 64-64

Skup
10th Croatian Biennial Echocardiography Congress with International Participation

Mjesto i datum
Poreč, Hrvatska, 16-18.05.2019

Vrsta sudjelovanja
Poster

Vrsta recenzije
Domaća recenzija

Ključne riječi
Fabry disease, myocardium, alpha-galactosidase

Sažetak
Introduction: Fabry disease is rare X-linked, recessive lysosomal storage disorder expressed as deficiency in enzyme α-galactosidase A that leads to progressive accumulation of globotriaosylceramide and related glycosphingolipids in various tissues. In cardiac tissues, progressive globotriaosylceramide accumulation leads to irreversible cardiac damage. Males are primarily affected by Fabry disease, but female heterozygotes may also have symptoms. Case report: Our patient is 47-years-old who has been suffering from chronic kidney disease since he was 23 years old. Only twelve years later he developed end-stage renal disease and has been undergoing regular haemodialysis in Dialysis Centre Prijedor (Bosnia and Herzegovina). He started his journey towards kidney transplantation in 2014 in University Hospital Centre Rijeka, which was performed in May 2018. In 2014, during pretransplantation workup, echocardiography was performed revealing concentric cardiac hypertrophy without left ventricle outflow tract obstruction (Figure 1 and Figure 2) associated with contractility and diastolic filling impairment. Following suspicion on Fabry disease, diagnosis was made by measuring α-galactosidase enzyme activity in leukocytes and molecular genetic testing of GLA gene mutation. Enzyme replacement therapy was started with intravenous infusion of recombinant α-galactosidase A (agalsidase beta). Conclusion: Renal disease and echocardiographic features of hypertrophic cardiomyopathy combined with electrocardiographic and clinical criteria should be considered as “red flags” for Fabry disease.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Ustanove
Medicinski fakultet, Rijeka,
Klinički bolnički centar Rijeka

Citiraj ovu publikaciju

Skorup, Lea; Grgić Romić, Ivana; Šimić, Jelena; Vujičić, Božidar; Rački, Sanjin; Ružić, Alen; Zaputović, Luka; Matana, Ante; Zaninović Jurjević, Teodora
The heart in Fabry’s disease // Cardiologia Croatica 2019 ; 14(3-4)
Zagreb: Hrvatsko kardiološko društvo, 2019. str. 64-64 doi:10.15836/ccar2019.64 (poster, domaća recenzija, prošireni sažetak, stručni)
Skorup, L., Grgić Romić, I., Šimić, J., Vujičić, B., Rački, S., Ružić, A., Zaputović, L., Matana, A. & Zaninović Jurjević, T. (2019) The heart in Fabry’s disease. U: Cardiologia Croatica 2019 ; 14(3-4) doi:10.15836/ccar2019.64.
@article{article, year = {2019}, pages = {64-64}, DOI = {10.15836/ccar2019.64}, keywords = {Fabry disease, myocardium, alpha-galactosidase}, doi = {10.15836/ccar2019.64}, title = {The heart in Fabry’s disease}, keyword = {Fabry disease, myocardium, alpha-galactosidase}, publisher = {Hrvatsko kardiolo\v{s}ko dru\v{s}tvo}, publisherplace = {Pore\v{c}, Hrvatska} }

Časopis indeksira:


  • Scopus


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