Create issue ticket

299 Possible Causes for Arteriosclerosis, Autosomal Dominant, Xanthoma

  • Hypercholesterolemia

    It predisposes to premature arteriosclerosis including coronary artery disease with heart attacks at an unusually young age.[] The xanthomas also regressed and disappeared by 3 years of age.[] RATIONALE: Autosomal-dominant hypercholesterolemia (ADH) is characterized by elevated low-density lipoprotein cholesterol levels and increased risk for coronary vascular disease[]

  • Heterozygous Familial Hypercholesterolemia

    Tendinous xanthomas, measured by quantitative xeroradiography, were significantly reduced (P Funding and Disclosures Supported by an Arteriosclerosis Specialized Centers of[] Sixty-two patients had positive physical examination findings for Achilles tendon xanthomas.[] 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.[]

  • 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[] The case presented here is of a 48-year old male with large tendon xanthomas attributable to CTX.[] Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an increase in low-density lipoprotein cholesterol[]

  • Homozygous Familial Hypercholesterolemia

    Arteriosclerosis (Suppl.) 9 , 1152–1157 (1989). 10 Gordon, B.R. et al .[] Physical examination revealed tuberous xanthomas on the processus olecrani, as well as smaller tendinous and tuberous xanthomas on the hands.[] Homozygous familial hypercholesterolemia (FH) is an autosomal dominant disease caused by a mutation in the low-density lipoprotein (LDL) receptor.[]

  • 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[] IIb or III hyperlipoproteinemia Hypercholesterolemia with endogenous hyperglyceridemia Hyperbetalipoproteinemia with prebetalipoproteinemia Tubo-eruptive xanthoma Xanthoma[] Dominant, Type B EnglishOMIM 144010 L6506378no S7518660 Y HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B EnglishMEDCIN 38631 L7070148no S8277886 Y familial defective apolipoprotein[]

  • 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.[] Hyperchylomicronemia LPL or Apo-CII deficiency (Can't breakdown TGs and Chylomicrons) Elevations in TGs and chylomicrons Decreased levels of LDL and HDL Risk of pancreatitis and xanthomas[] […] 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[]

  • Hypertriglyceridemia

    […] triglyceride concentration in the blood; an inherited form occurs in familial hyperlipoproteinemia IIb and hyperlipoproteinemia type IV; linked to higher risk of heart disease and arteriosclerosis[] Eruptive xanthomas are cutaneous lesions often indicating severe hypertriglyceridemia and uncontrolled diabetes.[] […] recessive inheritance of lipoprotein lipase deficiency; 0.0001% prevalence Familial combined hyperlipidemia (type IIb): usually autosomal dominant, caused by overproduction[]

  • Hyperlipoproteinemia Type 1

    Arteriosclerosis 1988; 8:742. PubMed Google Scholar 14. Klausen IC, Sjol A, Hansen PS, Gerdes LU, Moller L, Lemming L, et al.[] However, the exact mechanisms that induce xanthoma formation are less clear.[] Characterized by an isolated elevation in the plasma level of endogenously synthesized triglyceride carried in vldl; considered to be an autosomal dominant trait.[]

  • Hyperlipoproteinemia Type 3

    Arteriosclerosis, Thrombosis, and Vascular Biology . Retrieved from[] […] common of the xanthomas.[] […] recessive or autosomal dominant condition (that is, if the trait has been inherited from both parents).[]

  • Hyperlipoproteinemia Type 4

    […] triglyceride concentration in the blood; an inherited form occurs in familial hyperlipoproteinemia IIb and hyperlipoproteinemia type IV; linked to higher risk of heart disease and arteriosclerosis[] , tendinous xanthoma and planar xanthoma (intertriginous and xanthelesma-like lesions).[] Type IV hyperlipoproteinemia occurred in 33.3 per cent, and the mode of inheritance was autosomal dominant with incomplete penetrance.[]

Similar symptoms