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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.[medicinenet.com] The xanthomas also regressed and disappeared by 3 years of age.[ncbi.nlm.nih.gov] 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]

  • Heterozygous Familial Hypercholesterolemia

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

  • 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[ncbi.nlm.nih.gov] The case presented here is of a 48-year old male with large tendon xanthomas attributable to CTX.[ncbi.nlm.nih.gov] 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]

  • Homozygous Familial Hypercholesterolemia

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

  • 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[kidneycoach.com] IIb or III hyperlipoproteinemia Hypercholesterolemia with endogenous hyperglyceridemia Hyperbetalipoproteinemia with prebetalipoproteinemia Tubo-eruptive xanthoma Xanthoma[icd9data.com] Dominant, Type B EnglishOMIM 144010 L6506378no S7518660 Y HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B EnglishMEDCIN 38631 L7070148no S8277886 Y familial defective apolipoprotein[doctor.am]

  • 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.[link.springer.com] 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[quizlet.com] […] 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[dovemed.com]

  • 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[fpnotebook.com] Eruptive xanthomas are cutaneous lesions often indicating severe hypertriglyceridemia and uncontrolled diabetes.[ncbi.nlm.nih.gov] […] recessive inheritance of lipoprotein lipase deficiency; 0.0001% prevalence Familial combined hyperlipidemia (type IIb): usually autosomal dominant, caused by overproduction[unboundmedicine.com]

  • 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.[link.springer.com] However, the exact mechanisms that induce xanthoma formation are less clear.[dermatologyadvisor.com] Characterized by an isolated elevation in the plasma level of endogenously synthesized triglyceride carried in vldl; considered to be an autosomal dominant trait.[icd10data.com]

  • Hyperlipoproteinemia Type 3

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

  • 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[fpnotebook.com] , tendinous xanthoma and planar xanthoma (intertriginous and xanthelesma-like lesions).[ijdvl.com] Type IV hyperlipoproteinemia occurred in 33.3 per cent, and the mode of inheritance was autosomal dominant with incomplete penetrance.[nejm.org]

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