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380 Possible Causes for Arteriosclerosis, Cataract, Xeroderma

  • Diabetes Mellitus

    Considering this, we reviewed the principles and guidelines of managing cataract in patients with diabetes.[] Conclusions In men and women, most variables predicting future diabetes in the present study are also known to be important risk factors for cardiovascular disease and arteriosclerosis[] Hyaline arteriosclerosis, a characteristic pattern of wall thickening of small arterioles and capillaries, is widespread and is responsible for ischemic changes in the kidney[]

  • Cockayne Syndrome

    To describe cataracts in classic and early onset Cockayne syndrome (CS).[] In addition, arteriosclerosis in the brain and subdural hemorrhage have been reported in a few CS cases.[] […] whose clinical presentation of cutaneous photosensitivity and central nervous system dysfunction is strongly reminiscent of the DeSanctis-Cacchione syndrome (DCS) variant of xeroderma[]

  • Menopause

    […] working bladder and bowel Greater risk of Alzheimer's disease Poor skin elasticity (increased wrinkling) Poor muscle power and tone Some weakening in vision, such as from cataracts[] Copyright 2017 Sociedad Española de Arteriosclerosis. Publicado por Elsevier España, S.L.U. All rights reserved.[]

  • Ayerza Syndrome

    […] blood disorder NEC V78.9 specified type NEC V78.8 bronchitis, chronic V81.3 brucellosis V74.8 cancer - see Screening, malignant neoplasm cardiovascular disease NEC V81.2 cataract[] […] 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[] Sclerosis of the pulmonary arteries in chronic cor pulmonale, caused by primary pulmonary arteriosclerosis or primary pulmonary hypertension.[]

  • Progeria

    […] column and metacarpal joints with short stature, beaked nose and high-pitched voice, The ocular findings include: spontaneous bilateral dislocation of spherophakic mature cataracts[] Bilateral stenosis of carotid siphons was prominent, while systemic arteriosclerosis was unremarkable assessed by the ankle-brachial index, carotid ultrasound imaging and[] We propose that progerin accumulation results in disruption of functions of some replication and repair factors, causing the mislocalization of XPA (xeroderma pigmentosum[]

  • Werner Syndrome

    Here, we report a successful management of hypermature cataract in WS.[] 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[] XPG incision defects result in the cancer-prone syndrome xeroderma pigmentosum, whereas truncating mutations of XPG cause the severe postnatal progeroid developmental disorder[]

  • Tricho-Retino-Dento-Digital Syndrome

    Nails Hair Hair: pili canaliculi uncombable hair pili trianguli Genitourinary External Genitalia Male: hypospadias Skeletal Feet: brachydactyly Head And Neck Eyes: juvenile cataract[] [症]】*phlebarteriectasia 【動揺歩行】*swaying gait 【動脈炎】*arteritis 【動脈管開存症】*patent ductus arteriosus 【動脈狭窄】*arteriostenosis 【動脈筋腫症】*arteriomyomatosis 【動脈結石】*arteriolith 【動脈硬化症】*arteriosclerosis[] […] hypohidrotic dysplasia Tricho retino dento digital syndrome Tricho-dento-osseous syndrome Tricho-hepato-enteric syndrome Trichodermodysplasia dental alterations Trichodysplasia xeroderma[]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    The ectodermal traits are clearly seen as trichodysplasia, onychodysplasia, skin manifestations, and nuclear cataract.[] Steatorrhea Glomerulonephritis Focal segmental glomerulosclerosis Glomerulosclerosis Dentinogenesis imperfecta Abnormality of macular pigmentation Muscle weakness Premature arteriosclerosis[] […] pigmentosum, group A XPA Xeroderma pigmentosum, group C XPC Xeroderma pigmentosum, group D ERCC2 Xeroderma pigmentosum, group E, DDB-negative subtype DDB2 Xeroderma pigmentosum[]

  • Xeroderma Pigmentosum-Cockayne Syndrome Complex

    Ophthalmic pathology disclosed cataracts, iris and ciliary body atrophy, inner retinal atrophy and gliosis, retinal pigment epithelial atrophy, and optic nerve atrophy.[] […] generally develop into skin cancer, and also develop characteristic CS manifestations such as microcephaly, hydrocephalus, cachexia, premature aging, dwarfism, skin atrophy, arteriosclerosis[] A family with xeroderma pigmentosum-Cockayne syndrome complex Abstract Xeroderma pigmentosum-Cockayne syndrome complex is the coexistence of two genodermatoses, xeroderma[]

  • Autosomal Recessive Primary Microcephaly Type 10

    Dysmorphism-Neuropathy Syndrome Congenital Disorder Of Glycosylation, Type IIh Congenital Muscular Dystrophy, Fukuyama Type Congenital Osteogenesis Imperfecta-Microcephaly-Cataracts[] Aortic Aneurysm TGFBR2 Aortic Rupture ATP7A Aortic Valve, Calcification Of NOTCH1 Arnold-Chiari Malformation ERF Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 TGFB3 Arteriosclerosis[] […] pigmentosum group C,278720 POLH Xeroderma pigmentosum variant type,278750 XPA Xeroderma pigmentosum, group A, 278700 ERCC3 Xeroderma pigmentosum, group B, 610651 ERCC2 Xeroderma[]

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