Erschienen in:
26.11.2020 | Letter to the Editor
Late-onset of primary antiphospholipid syndrome: a case report
verfasst von:
Adam Benkirane, Bérangère Devalet, Pauline Montigny, Frédéric London
Erschienen in:
Acta Neurologica Belgica
|
Ausgabe 5/2021
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Excerpt
Antiphospholipid syndrome (APS) is a rare autoantibody-mediated acquired disorder characterized by thrombotic events and/or obstetrical morbidities, with persistent antiphospholipid (aPL) antibodies (Abs) [
1]. Its diagnosis requires persistent positivity in at least one of three aPL tests conducted on two or more occasions at least 12 weeks apart [
1]. APS is likely to be diagnosed in early adulthood and is far more common in women [
2,
3]. Onset of APS over the age of 50 is however rare [
4]. Here, we describe a case of late-onset of triple-positive primary APS. …