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201 Possible Causes for Arteriosclerosis, Congenital Pain Insensitivity

  • Heterozygous Familial Hypercholesterolemia

    insensitivity to pain with anhidrosis ) KIT ( KIT Piebaldism , Gastrointestinal stromal tumor ) STPK AMHR2 ( Persistent Müllerian duct syndrome II ) TGF beta receptors :[en.wikipedia.org] Tendinous xanthomas, measured by quantitative xeroradiography, were significantly reduced (P Funding and Disclosures Supported by an Arteriosclerosis Specialized Centers of[nejm.org] Corresponding author: Unidad Clínica y de Investigación en Lípidos y Arteriosclerosis, Hospital Universitario Miguel Servet, Avda.[revespcardiol.org]

  • Homozygous Familial Hypercholesterolemia

    insensitivity to pain with anhidrosis) KIT (KIT Piebaldism, Gastrointestinal stromal tumor) STPK AMHR2 (Persistent Müllerian duct syndrome II) TGF beta receptors: Endoglin[en.wikipedia.org] Arteriosclerosis (Suppl.) 9 , 1152–1157 (1989). 10 Gordon, B.R. et al .[nature.com] Arteriosclerosis. 1989;9:211-216. Raal FJ, Pappu AS, Illingworth DR, et al.[read.nxtbook.com]

  • Familial Hyperlipidemia

    insensitivity to pain with anhidrosis ) KIT ( KIT Piebaldism, Gastrointestinal stromal tumor ) STPK AMHR2 ( Persistent Müllerian duct syndrome II ) TGF beta receptors : Endoglin[en.wikipedia.org] ., 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] Familial hypercholesterolemia predisposes a person to premature arteriosclerosis, including coronary artery disease, and can lead to heart attacks at an unusually young age[medicinenet.com]

  • Ayerza Syndrome

    , see congenital insensitivity to pain asymmetric hypoplasia of facial structures, see craniofacial microsomia ataxia neuropathy spectrum ataxia telangiectasia syndrome, see[mygenomics.com] […] of the pulmonary arteries in chronic cor pulmonale; associated with severe cyanosis, it is a condition resembling polycythemia vera but resulting from primary pulmonary arteriosclerosis[medical-dictionary.thefreedictionary.com] Sclerosis of the pulmonary arteries in chronic cor pulmonale, caused by primary pulmonary arteriosclerosis or primary pulmonary hypertension.[definithing.com]

  • Pathological Fracture

    Congenital insensitivity to pain with anhidrosis (CIPA) is a rare hereditary sensory and autonomic neuropathy (HSAN) characterized by pain, self-mutilating behaviour, anhidrosis[ncbi.nlm.nih.gov] INTRODUCTION: Mönckeberg's sclerosis is a special form of arteriosclerosis characterized by calcification and ossification of the media of medium size arteries mainly of lower[ncbi.nlm.nih.gov]

  • Werner Syndrome

    Congenital Insensitivity to Pain with Anhidrosis Yasuhiro Indo. Initial Posting: August 5, 2008; Last Update: April 17, 2014.[ncbi.nlm.nih.gov] We present the neuropathological data of a 49-year-old patient with a history of Werner syndrome: The main features were arteriosclerosis of the small intracerebral arteries[ncbi.nlm.nih.gov] He also had severe arteriosclerosis of the coronary arteries (as identified by coronary arteriography) and the legs.[nejm.org]

  • Psychosomatic Disorder

    Anomalies/Mental Retardation Syndrome Congenital Pain Insensitivity Conn's syndrome Contiguous Abcd1/Dxs1375e Deletion Syndrome Corneal Cerebellar Syndrome Cornelia de Lange[rgd.mcw.edu] Heart disease-associated arteriosclerosis: Studies have concluded that the development of coronary heart disease is correlated with several risk factors in which depression[news-medical.net] […] syndrome congenital central hypoventilation syndrome congenital heart defects, hamartomas of tongue, and polysyndactyly Congenital Hypoplastic Anemia with Multiple Congenital[rgd.mcw.edu]

  • Primary Erythromelalgia

    Loss of function mutations lead to congenital insensitivity to pain.[ncbi.nlm.nih.gov] Multiple sclerosis • Plantar fasciitis • Reflex sympathetic dystrophy syndrome • Reflex sympathetic dystrophy syndrome • Acute gout • Bacterial cellulitis • Vasculitis • Arteriosclerosis[scielo.br] Our findings demonstrate that mutations encoding for DIV of Nav1.7 can not only be linked to congenital insensitivity to pain or paroxysmal extreme pain disorder but can also[ncbi.nlm.nih.gov]

  • Acroosteolysis

    insensitivity to pain; injury such as frostbite, thermal or electrical burns, or snake bite; trauma; psoriasis; congenital abnormality such as with Hadju-Cheney; metabolic[en.wikibooks.org] Common causes of acquired bone resorption include several vascular (arteriosclerosis obliterans, diabetic gangrene,Raynaud disease), inflammatory (psoriatic and rheumatoid[rrnursingschool.biz] […] obliterans Arteriosclerosis producing narrowing and occlusion of the arterial lumen; the resulting ischemia causes bone resorption Lesch-Nyhan syndrome Disorder characterized[radiologykey.com]

  • Lytic Bone Lesion

    , Congenital, Autosomal Recessive Asymbolia For Pain Congenital Analgesia, Autosomal Recessive Insensitivity To Pain, Channelopathy-Associated Neuropathy, Hereditary Sensory[ukgtn.nhs.uk] Common causes of acquired bone resorption include several vascular (arteriosclerosis obliterans, diabetic gangrene,Raynaud disease), inflammatory (psoriatic and rheumatoid[rrnursingschool.biz] NCI] ARPKD Arrhythmias and Sexual Activity Arrhythmias: Foods That Affect Heart Rate Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) ARSA Arteriohepatic Dysplasia Arteriosclerosis[healthmedicinet.com]

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