prikaz prve stranice dokumenta Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl
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Scientific paper - Preliminary note / Short communication
Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl
Rheumatology International, 33 (2013), 5; 1359-1362. https://doi.org/10.1007/s00296-011-2300-5
Jelušić, Marija; Starčević, Katarina; Vidović, Mandica; Dobrota, Savko; Potočki, Kristina; Banfić, Ljiljana; Anić, Branimir

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Jelušić, M., Starčević, K., Vidović, M., Dobrota, S., Potočki, K., Banfić, Lj. & Anić, B. (2013). Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl. Rheumatology International, 33. (5), 1359-1362. doi: 10.1007/s00296-011-2300-5

Jelušić, Marija, et al. "Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl." Rheumatology International, vol. 33, no. 5, 2013, pp. 1359-1362. https://doi.org/10.1007/s00296-011-2300-5

Jelušić, Marija, Katarina Starčević, Mandica Vidović, Savko Dobrota, Kristina Potočki, Ljiljana Banfić and Branimir Anić. "Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl." Rheumatology International 33, no. 5 (2013): 1359-1362. https://doi.org/10.1007/s00296-011-2300-5

Jelušić, M., et al. (2013) 'Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl', Rheumatology International, 33(5), pp. 1359-1362. doi: 10.1007/s00296-011-2300-5

Jelušić M, Starčević K, Vidović M, Dobrota S, Potočki K, Banfić Lj, and sur.. Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl. Rheumatology International [Internet]. 2013 May [cited 2024 November 22];33(5):1359-1362. doi: 10.1007/s00296-011-2300-5

M. Jelušić, et al., "Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl", Rheumatology International, vol. 33, no. 5, pp. 1359-1362, May 2013. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:105:392493. [Accessed: 22 November 2024]

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Metadata
Title (english)Familial antiphospholipid syndrome presenting as bivessel arterial occlusion in a 17-year-old girl
AuthorMarija Jelušić
AuthorKatarina Starčević
AuthorMandica Vidović
AuthorSavko Dobrota
AuthorKristina Potočki
AuthorLjiljana Banfić
AuthorBranimir Anić
Author's institutionUniversity of Zagreb
School of Medicine
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Abstract (english)
This article presents a case of a 17-year-old girl with primary antiphospholipid syndrome developing subacute signs of hand and leg ischaemia caused by radiologically verified radial and popliteal artery occlusion. She is successfully treated with a thrombolytic agent (alteplase) and recovers completely. Her laboratory results came positive for all three subtypes of antiphospholipid antibodies. This kind of antiphospholipid syndrome presentation is a very rare entity in itself. Shortly afterwards her mother is diagnosed with primary antiphospholipid syndrome as well. A familial form of antiphospholipid syndrome is suspected. Combination of a familial antiphospholipid syndrome presenting as bivessel arterial thrombosis is a unique case, to the best of our knowledge, never described in the literature before.
Keywords (english)
Languageenglish
Publication typeScientific paper - Preliminary note / Short communication
Publication statusPublished
Peer reviewPeer review
Publication versionAccepted version
Journal titleRheumatology International
Numberingvol. 33, no. 5, pp. 1359-1362
p-ISSN0172-8172
DOIhttps://doi.org/10.1007/s00296-011-2300-5
URN:NBNurn:nbn:hr:105:392493
Publication2013-05
Document URLhttp://doi.org/10.1007/s00296-011-2300-5
Type of resourceText
Access conditionsOpen access
Terms of useLicence In copyright icon
Created on2024-03-28 08:02:42