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EditorialEditorial
Open Access

Hughes’ antiphospholipid syndrome; 40 years on

Ali S. Jawad
Saudi Medical Journal November 2023, 44 (11) 1071-1072; DOI: https://doi.org/10.15537/smj.2023.44.11.20230725
Ali S. Jawad
From William Harvey Research Institute, Queen Mary University of London, and from the Royal London Hospital, London, United Kingdom.
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    Table 1

    - Other clinical manifestations of antiphospholipid syndrome.

    SystemsClinical features
    NeurologicChoreoathetosis, cognitive decline, migraine, myelitis, retinal ischemia, and seizures
    CardiovascularAccelerated atherosclerosis, aortic and mitral valve thickening, cardiomyopathy, and non-infectious vegetations
    PulmonaryDiffuse alveolar haemorrhage, pulmonary hypertension
    RenalAPS nephropathy, renal artery stenosis
    EndocrineAdrenal insufficiency
    HaematologicAutoimmune haemolytic anaemia, bleeding (due to hypothrombonemia), Evans syndrome, and thrombocytopenia
    ArticularArthralgia, arthritis, and avascular necrosis
    CutaneousDigital ischemia, livedo racemosa/reticularis, livedoid vasculopathy, and splinter haemorrhages

    APS: antiphospholipid syndrome

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    Saudi Medical Journal: 44 (11)
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    1 Nov 2023
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    Hughes’ antiphospholipid syndrome; 40 years on
    Ali S. Jawad
    Saudi Medical Journal Nov 2023, 44 (11) 1071-1072; DOI: 10.15537/smj.2023.44.11.20230725

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    Hughes’ antiphospholipid syndrome; 40 years on
    Ali S. Jawad
    Saudi Medical Journal Nov 2023, 44 (11) 1071-1072; DOI: 10.15537/smj.2023.44.11.20230725
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