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2,673 Possible Causes for Acute Myocardial Infarction, Autosomal Dominant

  • Hypercholesterolemia

    RATIONALE: Autosomal-dominant hypercholesterolemia (ADH) is characterized by elevated low-density lipoprotein cholesterol levels and increased risk for coronary vascular disease[ncbi.nlm.nih.gov] Lipid profiles are best avoided following acute myocardial infarction, for up to three months, although cholesterol can be in the first 24 hours.[beta.labcorp.com] Severe hypercholesterolemia associated or not with xanthomas in a child may suggest the diagnosis of homozygous autosomal dominant hypercholesterolemia (ADH), autosomal recessive[ncbi.nlm.nih.gov]

  • Heterozygous Familial Hypercholesterolemia

    HeFH is an autosomal dominant disorder; if one inherits the mutated gene that causes high cholesterol levels from only one parent, HeFH will be inherited.[patientworthy.com] Indeed, acute myocardial infarction and sudden cardiac death are the primary causes of mortality among those with HeFH.[symptoma.com] In this autosomal dominant disease, the concentration of plasma low-density lipoprotein cholesterol (LDL-C) is strongly elevated since birth.[mdpi.com]

  • Familial Hypercholesterolemia

    Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an increase in low-density lipoprotein cholesterol[ncbi.nlm.nih.gov] The proband presented with an acute myocardial infarction at age 43.[ncbi.nlm.nih.gov] Abstract Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an increase in low-density lipoprotein cholesterol[doi.org]

  • Hypertrophic Cardiomyopathy

    This report describes the novel sampling of autosomal dominant polycystic kidney disease (ADPKD) combined with hypertrophic cardiomyopathy (HCM).[ncbi.nlm.nih.gov] HCM was also associated with a higher incidence of myocardial infarction ([MI] 1.90 [1.27-2.84]) and coronary revascularisation (2.32 [1.46-3.69]).The absolute Kaplan-Meier[ncbi.nlm.nih.gov] Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease with variable clinical features that is inherited as autosomal dominant with variable penetrance[ncbi.nlm.nih.gov]

  • Cardiomyopathy

    A novel autosomal-dominant in-frame deletion resulting in a nonsense mutation in the desmoplakin (DSP) gene was identified in association with biventricular arrhythmogenic[ncbi.nlm.nih.gov] Acute myocarditis may clinically mimic an acute myocardial infarction with chest pain.[radiologyassistant.nl] AD, AD 14 SLC25A4 103220 Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 2; mitochondrial DNA depletion syndrome 12; mitochondrial[centogene.com]

  • Homozygous Familial Hypercholesterolemia

    Homozygous familial hypercholesterolemia (FH) is an autosomal dominant disease caused by a mutation in the low-density lipoprotein (LDL) receptor.[ncbi.nlm.nih.gov] One patient who refused LA during pregnancy died from acute myocardial infarction after delivery.[ncbi.nlm.nih.gov] Familial hypercholesterolemia is an autosomal dominant disease in which the gene encoding the low density lipoprotein receptor is defective.[ncbi.nlm.nih.gov]

  • Hypertension

    Liddle’s Syndrome This is an autosomal dominant form of monogenic hypertension that results from mutations in the amiloride-sensitive epithelial sodium channel, leading to[web.archive.org] They have shown long-term beneficial effects on mortality and cardiovascular disease (CVD) when used in people with heart failure or acute myocardial infarction.[ncbi.nlm.nih.gov] There was no trial that included exclusively patients with acute aortic dissection or acute myocardial infarction.[doi.org]

  • Tumor Necrosis Factor Receptor 1-associated Periodic Syndrome

    Periodic fever, familial, autosomal dominant. Online Mendelian Inheritance in Man (OMIM). 7.[springerlink.com] An increased risk of atherosclerosis and acute myocardial infarction has been noted.[orpha.net] The TNF-receptor-associated periodic syndrome (TRAPS) is an autosomal dominant auto-inflammatory disorder, characterized by recurrent febrile attacks and localized inflammation[ncbi.nlm.nih.gov]

  • Pheochromocytoma

    VHL is an autosomal dominant disorder that is characterized by a predisposition to multiple tumors, including retinal and central nervous system hemangioblastomas, renal cell[ncbi.nlm.nih.gov] This 16-year-old boy presented with acute retrosternal pain possibly representing acute myocardial infarction. Cardiac enzymes were within reference ranges.[ncbi.nlm.nih.gov] Pheochromocytoma and paraganglioma (PPGL) are rare autosomal dominant disorders derived from the neural crest chromaffin tissues of the autonomic nervous system.[ncbi.nlm.nih.gov]

  • Diabetes Mellitus

    In autosomal dominant inheritance, a child who has a parent with a mutation has a 50% chance of inheriting that mutation. Autosomal recessive.[web.archive.org] The objective of this study was to analyze the significance of hs-CRP in type 2 diabetes mellitus (T2DM) combined with acute myocardial infarction (AMI).Fifty patients with[ncbi.nlm.nih.gov] Patient was on hemodialysis due to the stage 5 chronic kidney failure and had various comorbid conditions: arterial hypertension, history of acute myocardial infarction, dilative[ncbi.nlm.nih.gov]

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