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2,746 Possible Causes for fabri, fabricando, fimus

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  • Fabry Disease

    […] angiokeratoma FD Gla Deficiency FABRY DISEASE edit English Fabry disease human disease Fabry's disease Anderson-Fabry disease angiokeratoma corporis diffusum alpha-galactosidase[wikidata.org] Fabry disease, also known as Anderson-Fabry disease, angiokeratoma corporis diffusum and alpha-galactosidase A deficiency, is a rare genetic lysosomal storage disorder.[symptoma.com] Fabry Disease. 2002 Aug 5 [updated 2017 Jan 5].[ghr.nlm.nih.gov]

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  • Alpha-Galactosidase

    Fabry disease is a rare but important cause of end-stage renal disease.[ncbi.nlm.nih.gov] Cerebrovascular symptoms with predominant affection of the vertebrobasilar circulation are one of the major sources of morbidity in Fabry's disease.[ncbi.nlm.nih.gov] Our case emphasizes the importance of ophthalmological findings in Fabry disease.[ncbi.nlm.nih.gov]

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  • Angiokeratoma Circumscriptum

    Angiokeratoma Corporis Circumscriptum (Fabry) definition Vascular malformation characterized by dilation of superficial vessels of the dermis and hyperkeratosis of the overlying[dermis.net] Additional studies, namely biochemical and molecular biological analyses, may be indicated to rule out Fabry disease.[symptoma.com] The systemic form of angiokeratoma is associated with Fabry disease and fucosidosis. There are several localized forms. Tongue involvement is uncommon.[ncbi.nlm.nih.gov]

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  • Restrictive Cardiomyopathy

    However, other infiltrative diseases (i.e. metabolic myopathies, Gaucher, Hunter's, and Hurler's diseases) or storage cardiomyopathies (haemochromatosis, Fabry's disease,[ncbi.nlm.nih.gov] Sarcoidosis and Fabry disease can infiltrate the nodal conduction region.[symptoma.com] Risk Factors Family history of RCM Inherited diseases (such as hereditary hemochromatosis, Fabry disease, mutant-type [hereditary] TTR amyloidosis, etc.)[unboundmedicine.com]

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  • Left Ventricular Hypertrophy

    We report the case of a rare cardiac presentation of Fabry disease.[ncbi.nlm.nih.gov] This case report shows that Anderson-Fabry disease may cause an apical form of left ventricular hypertrophy.[ncbi.nlm.nih.gov] Patients with Fabry disease (FD) develop progressive left ventricular hypertrophy (LVH).[ncbi.nlm.nih.gov]

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  • Common Cold

    Acta Paediatr Scand Suppl 1985;319:158-63. [ PubMed abstract ] Fabris N, Mocchegiani E. Zinc, human diseases and aging.[ods.od.nih.gov]

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  • Infiltrative Cardiomyopathy

    Fabry’s disease) early diagnosis can result in potentially curative treatment.[link.springer.com] This biomarker has not been fully evaluated in Fabry disease.[bmccardiovascdisord.biomedcentral.com] disease in 3 patients) and 35 HCM patients.[ncbi.nlm.nih.gov]

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  • Hypertrophic Cardiomyopathy

    KEYWORDS: AV node ablation; Fabry disease; Hypertrophic cardiomyopathy; Sudden death[ncbi.nlm.nih.gov] BACKGROUND: Fabry disease (FD) and hypertrophic cardiomyopathy (HCM) are two diseases with a different pathophysiology, both cause left ventricular hypertrophy (LVH) and myocardial[ncbi.nlm.nih.gov] Abstract Purpose To compare left ventricular (LV) and right ventricular (RV) 3.0-T cardiac magnetic resonance (MR) imaging T1 values in Anderson-Fabry disease (AFD) and hypertrophic[ncbi.nlm.nih.gov]

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  • Schindler Disease

    Fabry disease, also known as Anderson-Fabry disease , is a multisystem disorder resulting from an X-linked inborn error of metabolism.[radiopaedia.org] Fabry or Anderson‐Fabry disease? The dermatologists William Anderson in the UK and Johannes Fabry in Germany were the first to describe Anderson‐Fabry disease.[academic.oup.com] disease, due to different lysosomal enzyme defects or unknown factors (see these terms).[orpha.net]

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  • Raynaud Phenomenon

    Abstract Fabry disease (FD) is a lysosomal disorder leading to progressive systemic involvement, including microvascular damage that leads to neurological and cardiovascular[ncbi.nlm.nih.gov] This syndrome includes acromegaly, Fabry's disease, pheochromocytoma (PCC), pulmonary adenocarcinoma, carpal tunnel syndrome (CTS), and myxedema.[symptoma.com] Prevalence of Raynaud phenomenon and nailfold capillaroscopic abnormalities in Fabry disease: a cross-sectional study. Medicine (Baltimore). 2015 May. 94 (20):e780.[emedicine.medscape.com]

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