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1,146 Possible Causes for Arteriosclerosis, Autosomal Dominant

  • Hypercholesterolemia

    It predisposes to premature arteriosclerosis including coronary artery disease with heart attacks at an unusually young age.[] RATIONALE: Autosomal-dominant hypercholesterolemia (ADH) is characterized by elevated low-density lipoprotein cholesterol levels and increased risk for coronary vascular disease[] Miettinen T (2018) Polymorphisms of the Genes Encoding Apoproteins A-I, B, C-III, and E and LDL Receptor, and Cholesterol and LDL Metabolism During Increased Cholesterol Intake, Arteriosclerosis[]

  • Heterozygous Familial Hypercholesterolemia

    Tendinous xanthomas, measured by quantitative xeroradiography, were significantly reduced (P Funding and Disclosures Supported by an Arteriosclerosis Specialized Centers of[] 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.[] Corresponding author: Unidad Clínica y de Investigación en Lípidos y Arteriosclerosis, Hospital Universitario Miguel Servet, Avda.[]

  • Familial Hypercholesterolemia

    METHODS: A total of 2685 FH patients, with a minimum follow-up of 6 months, included in the Dyslipidemia Registry of the Spanish Arteriosclerosis Society, were sorted according[] Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an increase in low-density lipoprotein cholesterol[] Abstract Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an increase in low-density lipoprotein cholesterol[]

  • Familial Hyperlipidemia

    ., 1984, Apoproteins B and AI and coronary artery disease in humans, Arteriosclerosis 4:79–83. PubMed CrossRef Google Scholar Chait, A., and Brunzell, J.[] […] with FCH Chromosome locus (specific region) 1q21-q23 has been linked to FCH APOA5 gene association with APOA1/CIII/AIV has also been linked to FCH Autosomal dominant: Autosomal[] Familial hypercholesterolemia predisposes a person to premature arteriosclerosis, including coronary artery disease, and can lead to heart attacks at an unusually young age[]

  • Homozygous Familial Hypercholesterolemia

    Arteriosclerosis (Suppl.) 9 , 1152–1157 (1989). 10 Gordon, B.R. et al .[] Homozygous familial hypercholesterolemia (FH) is an autosomal dominant disease caused by a mutation in the low-density lipoprotein (LDL) receptor.[] Arteriosclerosis. 1989;9:211-216. Raal FJ, Pappu AS, Illingworth DR, et al.[]

  • Hyperlipoproteinemia Type 2b

    Well, there are a number of reasons, and they are as follows: • Arteriosclerosis – the kidneys have a role in regulating calcium levels, when this diminishes calcium build[] Dominant, Type B EnglishOMIM 144010 L6506378no S7518660 Y HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B EnglishMEDCIN 38631 L7070148no S8277886 Y familial defective apolipoprotein[] Arteriosclerosis 7 : 483 –490, 1987 Krauss RM, Williams PT, Lindgren FT, Wood PD: Coordinate changes in levels of human serum low and high density lipoprotein subclasses in[]

  • Hypertension

    When the hypertensinogenic factor cannot be reduced or eliminated, as with systolic hypertension induced by aging (arteriosclerosis), recognition of the underlying cause of[] […] hypertensive syndromes glucocorticoid-remediable aldosteronism (GRA), Liddle’s syndrome, and apparent mineralocorticoid excess have been identified, whereas in a fourth, autosomal[] 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[]

  • Binswanger Disease

    Synonyms: Binswanger disease a.k.a. subcortical arteriosclerosis encephalopathy: Diagnosis: MRI T2/FLAIR: subcortical white matter hyperintensities in confluent areas (initially[] A genetically transmitted form of the disease is known as familial arteriopathic leukoencephalopathy or CADASIL (cerebral autosomal dominant arteriopathy with subcortical[] Signs and Symptoms Nystagmus Abnormality of extrapyramidal motor function Alopecia Arteriosclerosis of small cerebral arteries Ataxia Autosomal recessive inheritance Babinski[]

  • Amyloidosis

    dominant hereditary polyneuropathy related to the organ deposition of mutant forms of the transthyretin protein (encoded by mutated TTR ) over time.[] BACKGROUND: Hereditary transthyretin amyloidosis is an autosomal dominant inherited disorder, first described in families with sensorimotor and autonomic neuropathy.[] The autosomal dominant transmission of HCM implies that many relatives are at risk for HCM associated morbidity and mortality, therefore genetic testing and counselling is[]

  • Familial Paget Disease of Bone

    Hultgren reported that there was an association between PDB and aortic stenosis, arteriosclerosis and intracardiac calcification [ 32 ].[] It is usually inherited in an autosomal dominant manner with incomplete penetrance.[] One study has shown that aortic stenosis, arteriosclerosis, and intracardiac calcifications are more common than in age-matched controls ( 24 ).[]

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