Pregled bibliografske jedinice broj: 400816
Amaurosis fugax caused by hereditary thrombophilia due to mutation of gene
Amaurosis fugax caused by hereditary thrombophilia due to mutation of gene // Bratisl Lek Listy, 110 (2009), (4); 245-246 (recenziran, članak, stručni)
CROSBI ID: 400816 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Amaurosis fugax caused by hereditary thrombophilia due to mutation of gene
Autori
Titlić, Marina ; Bradić-Hammoud, Mirna ; Miric, Lina
Izvornik
Bratisl Lek Listy (0006-9248) 110
(2009), (4);
245-246
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, stručni
Ključne riječi
amaurosis fugax; thrombophilia; hereditary
Sažetak
We are presenting a 59-year old woman and 37- year old man with amaurosis fugax. They underwent a comprehensive ophthalmological and neurological examination. Standard diagnostic examination revealed no possible cause of this temporary condition, therefore additional genetic analysis for possible hereditary thrombophilia was performed. Examination established hereditary thrombophilia: the heterozygotic type gene for MTHFR (C677), deletion/insertion polymorphism for PAI-1 (4G/5G) in women and deletion/insertion polymorphism 4G/5G for PAI-1 and heterozygotic genotype DD (190 bp) for angiotensin converting enzyme (ACE) in man. In our patients, amaurosis fugax is probably caused by hereditgary thrombophilia.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
216-0000000-0525 - Rana dijagnostika i trombolitičko liječenje ishemijskog moždanog udara (Janković, Stipan, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Split
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
