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  • Fabry disease

    ...deficiency Anderson-Fabry disease Angiokeratoma corporis diffusum Diffuse angiokeratoma FD Prevalence 1-5 / 10 000...characteristic neurological (pain), cutaneous (angiokeratoma), renal (proteinuria, kidney failure...

    Orphanet, 01 March 2012

  • Enzyme replacement therapy for Anderson-Fabry disease

    ...Disease) OR (Disease, Fabry) OR (Angiokeratoma Corporis Diffusum) OR (Anderson...numbness of the hands and forearms Angiokeratoma Skin condition characterized by...there is thickening of the epidermis Angiokeratoma corporis diffusum X-linked disorder...

    Cochrane Database of Systematic Reviews, 28 February 2013 - Publisher: John Wiley & Sons, Ltd

  • Enzyme replacement therapies for Fabry s disease and mucopolysaccharidosis type 1

    ...0 appearance Yes 1 Mild 1 Severe 2 Angiokeratoma No 0 Vertigo No 0 Some 1 Mild 1 Extensive...Hearing Pulmonary (years) involvement angiokeratoma anhydrosis loss involvement...cerebrovascular symptoms, neuropathic pain, angiokeratoma, hypertension and hyperlipidaemia...

    NIHR Journals Library - Health Technology Assessment, 12 February 2013

  • Campbell de Morgan Spot

    ...Differential diagnosis [3] Malignant melanoma Spider naevi Pyogenic granuloma Kaposi's sarcoma Insect bite Angiokeratoma Congenital haemangioma Primary care management Reassure - these lesions usually require no treatment. If removal...

    Patient UK

  • Migalastat for Fabry disease: update at NIHR Horizon Scanning Centre

    ...in UK males it takes a mean of 8.18 years from onset of neuropathic pain and a mean of 10.70 years from the onset of angiokeratoma to achieve a diagnosis. Although clinically heterogenous, classical Fabry disease is usually a slowly progressive disease...

    NIHR Horizon Scanning Centre, 10 April 2014

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