GEMdatabase - Selected Title TITLE cerebrotendinous xanthomatosis. DATE July 2003. COST CONDITIONS CerebrotendinousXanthomatosis, Metabolic Disorders, Mitochondrial Disorders. SUBJECTS http://www.gemdatabase.org/GEMDatabase/TitleDetailsOne.asp?TitleID=849
GEMdatabase - Browse Titles cerebrotendinous xanthomatosis This review focuses on the diagnosis, management,and genetic counseling of patients and families with cerebrotendinous http://www.gemdatabase.org/GEMDatabase/BrowseTitles.asp?curpage=6
Cerebrotendinous Xanthomatosis In A Family RG Kar Medical College, Calcutta700004. cerebrotendinous xanthomatosisin a family. Indian Journal of Dermatology. 1999 Jul-Sep; 44(3) 153-6. http://medind.nic.in/imvw/imvw5716.html
Extractions: Extracted from IndMED Chatterjee G; Chakraborty I; Das TK; Datta C R.G. Kar Medical College, Calcutta-700004 Cerebrotendinous xanthomatosis in a family Indian Journal of Dermatology. 1999 Jul-Sep; 44(3): 153-6 ABSTRACT: A family consisting of a brother (11 years) and his twin sisters (13 years) with cerebrotendinous xanthomatosis is presented. The brother had bilateral achilles tendon xanthoma, low intelligence, poor memory with early cerebellar signs. The sisters had bilateral juvenile cataracts in addition to achilles tendon xanthomas. The serum cholesterol level in all the three was within normal limits. The FNAC and histopathology of tendinous swelling showed touton giant cells and foam cells. A diagnosis of cerebrotendinous xanthomatosis was made on the basis of achilles tendon xanthomas, bilateral cataracts and normal serum cholesterol. KEYWORDS: Xanthomatosis, Cerebrotendinous/DI; Xanthomatosis, Cerebrotendinous/PA; Cataract; Achilles Tendon/PA; Cholesterol/BL; Central Nervous System/PP; Bile Acids and Salts; Hydroxylases/DF; Biopsy; Case Report; Child; Adolescence; Male; Female; Human References: 9 Record Identifier: NI201272
Journal Of Arthroplasty And Arthroscopic Surgery 12, No1 (9193), 2001 cerebrotendinous xanthomatosis. cerebrotendinous xanthomatosisis a rare metabolic disease of autosomal recessive inheritance. http://arthroplasty-arthroscopy.mc.metu.edu.tr/2001/no1-16.html
Extractions: Fatih EKSIOGLU, Eftal GUDEMEZ, Onder BOZDOGAN, Deniz ALTINOK, Sedat ULKATAN Cerebrotendinous Xanthomatosis is a rare metabolic disease of autosomal recessive inheritance. Clinical findings include, tendon xanthoma, cataract, neurological dysfunction, ataxia, dementia, slightly high serum cholesterol levels. We report a case aged 17 had painless, semimobile, solid masses on her both achilles tendon diagnosed as Cerebrotendinous xanthomatosis. Cerebrotendinous xanthomatosis must be considered in the diagnosis of patients with tendon xanthoma, cataract, neurological dysfunction, ataxia, dementia, slightly high serum cholesterol levels. Key Words : Cerebrotendinous Xanthomatosis, Achilles Tendon. BACK TO INDEX PAGE
Program Nr 679 Program Nr 679 cerebrotendinous xanthomatosis(CTX). The first mexicanfamily reported. IA Gamboa 1 , CF Salinas 2 , R. Mendivil http://www.faseb.org/genetics/ashg00/f679.htm
Xanthoma cerebrotendinous xanthomatosis a rare disease with diverse manifestations. Thisminireview deals with a new appraisal of cerebrotendinous xanthomatosis. http://www.thedoctorsdoctor.com/diseases/xanthoma.htm
Extractions: Benign fibrohistiocytoma (xanthomatous variant) of the acromion. A case report and review of the literature. Macdonald D, Fornasier V, Holtby R. Arch Pathol Lab Med 2002 May;126(5):599-601Abstract quote A number of fibrous lesions involving bone display almost identical histologic appearances yet may represent either reactive or neoplastic conditions, resulting in a confusing nomenclature and possible diagnostic confusion. We report the case of a young man with no significant previous medical history who presented with a painful lesion in the left shoulder, which consisted almost entirely of xanthomatous material. We discuss the possible differential diagnosis of this lesion and why benign fibrous histiocytoma is the preferred terminology for this lesion.
Cerebrotendinous Xanthomatosis From Linkspider UK Health Directory cerebrotendinous xanthomatosis by Linkspider UK, cerebrotendinous xanthomatosislinks and cerebrotendinous xanthomatosis topics from our Health directory. http://linkspider.co.uk/Health/ConditionsandDiseases/NutritionandMetabolismDisor
Extractions: Match » -All words -Any word -Exact text Search » The Web Jobs / Vacancy Images / Photos FTP / Downloads United Kingdom United States of America Argentina Austria Australia Bangladesh Belgium Bolivia Brazil Bulgaria Canada Chile China Cuba Cyprus Czech Republic Czechoslovakia Denmark Dominican Republic Ecuador Egypt Estonia Finland France Germany Ghana Greece Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Jordan Kenya Kuwait Latvia Lithuania Luxembourg Malaysia Malta Mexico Moldavia Monaco Morocco Mozambique Nepal Netherlands New Zealand Nicaragua Nigeria North Korea Norway Pakistan Panama Paraguay Peru Philippines Poland Portugal Qatar Romania Russian Federation Saudi Arabia Singapore South Africa South Korea Spain Sri Lanka Sweden Switzerland Taiwan Tanzania Thailand Tunisia Turkey Ukraine United Arab Emirates Uruguay Venezuela Yemen Yugoslavia Zambia Zimbabwe Ranking » On (no duplicate) Off (allow duplicate) Add my Site Toolbar Affiliates See Also: Health: Conditions and Diseases: Musculoskeletal Disorders: Connective Tissue
Dictionary Definition Of CEREBROTENDINOUS XANTHOMATOSIS www.dictionarybarn.com/XANTHOMATOSISCEREBROTENDINOUS.php More results from www.dictionarybarn.com Clinical Trial Phase II Study of Cholesterol- and Cholestanol Phase II Study of Cholesterol- and Cholestanol-Free Diet, Lovastatin,and Chenodeoxycholic Acid for cerebrotendinous xanthomatosis. http://www.dictionarybarn.com/CEREBROTENDINOUS-XANTHOMATOSIS.php
Extractions: A disorder with deposition of cholestanol in the brain and other tissues and high levels in plasma but with normal cholesterol level; characterised by progressive cerebellar ataxia beginning after puberty, juvenile cataracts, spinal cord involvement, and tendinous or tuberous xanthomata; autosomal recessive inheritance. Probably due to a defect in hepatic mitochondrial 26-hydroxylase in bile acid biosynthesis.
Endotext.com - Diseases Of Bone And Calcium Metabolism, Ch 9 Bibliography Hsieh, CL, Francke, U., Russell, DW 1991 Mutations in the bile acid biosyntheticenzyme sterol 27hydroxylase underlie cerebrotendinous xanthomatosis J Biol http://www.endotext.org/parathyroid/parathyroid3/parathyroidbiblio3.htm
Extractions: 1. Whistler, D. 1645 De morbo puerli anglorum, quem patrio ideiomate indigenae vocant "the rickets" J Hist Med;5:397-415. 2. Mellanby, E. 1919 An experimental investigation on rickets. Lancet;1:407-412. 3. McCollum, E.V., Simmonds, N., Becker, J.E., Shipley, P.G. 1922 An experimental demonstration of the existence of a vitamin which promotes calcium deposition J Biol Chem;53:293-298. 4. Steenbock, H., Black, A. 1924 Fat-soluble vitamins. XVII. The induction of growth-promoting and calcifying properties in a ration by exposure to ultraviolet light J Biol Chem;61:405-422. 5. Huldshinsky, K. 1919 Heilung von rachitis durch kunstalich hohensonne Deut Med Wochenschr;45:712-713. 6. Hess, A.F., Unger, L.F. 1921 Cure of infantile rickets by sunlight J Am Med Assoc;77:39. 7. F.A., A., Bourdillon, R.B., Bruce, H.M., Jenkins, R.G.C., Webster, T.A. 1931 The distillation of vitamin D Proc R Soc;B107:76-90. 8. Windaus, A., Schenck, F., von Werder, F. 1936 Uber das antirachitisch wirksame bestrahlungs-produkt aus 7-dehydro-cholesterin. Hoppe-Seylers Z Physiol Chem;241:100-103. 9. Holick, M.F., Richtand, N.M., McNeill, S.C., Holick, S.A., Henley, J.W., J.T., P.J. 1979 Isolation and identification of previtamin D3 from the skin of exposed to ultraviolet irradiation Biochemistry;18:1003-1008.
1998 - Journal Of Dermapathology Özet cerebrotendinous xanthomatosis (CTX) tanisi alan 43 yasindaki erkekhastanin 25 senedir sol topukta asil tendonu üzerinde ve diz altinda, 4 http://www.ato.org.tr/konuk/tdp/tjod/1998-01/9852.html
Extractions: Cerebrotendinous xanthomatosis (CTX) tanýsý alan 43 yaþýndaki erkek hastanýn 25 senedir sol topukta aþil tendonu üzerinde ve diz altýnda, 4 senedir sað topukta aþil tendonu üzerinde ve sað dizde semimobil ve aðrýsýz kitleleri mevcuttu. Oldukça nadir olan ve otozomal resessif olarak geçen CTX'in klinik bulgularý; tendinöz ksantomalar, katarakt, nörolojik fonksiyon bozukluðu, demans, ataksi, hafifçe yüksek serum kolesterol seviyesi ve koroner arter hastalýðýdýr. Çoðunlukla lezyonlar el ve ayakta ekstensör tendonlarýn üzerinde ortaya çýkabileceði gibi aþil ve patella tendonlarý da tutulabilmektedir.
Extractions: Research Paper Title Coexpression of glucose transporter 1 and matrix metalloproteinase-2 in human cancers. Source J. Natl. Cancer Inst. 94:1080-1091 Year Title Overexpression of ornithine decarboxylase enhances endothelial proliferation by suppressing endostatin expression. Source Blood 99 :1478-1481 Year Title Allopurinol suppresses paranonylphenol and 1-methyl-4-phenylpyridinium ion-induced hydroxyl radical generation in rat striatum.
Extractions: Coexpression of glucose transporter 1 and matrix metalloproteinase-2 in human cancers. J. Natl. Cancer Inst. 94:1080-1091 Overexpression of ornithine decarboxylase enhances endothelial proliferation by suppressing endostatin expression. Blood 99 :1478-1481 Allopurinol suppresses paranonylphenol and 1-methyl-4-phenylpyridinium ion-induced hydroxyl radical generation in rat striatum. Neurosci.Lett. 306 :9-12 Anti-alpha integrin antibody induces secretion and activation of 72 kDa progelatinase by human fibroblasts. Biochem.Mol.Biol.Int. 51: 1-7 Antisense oligonucleotides targetted to midkine, a heparin-binding growth factor, suppresses tumorigenicity of mouse rectal carcinoma cells. Cancer Res.61:8486-8491 Calreticulin is directly involved in anti-a3 integrin antibody-mediated secretion and activation of matrix metalloprotease-2. Biochem.Biophys.Res. Commun. 283: 297-302 Frontal lobe dementia with abnormal cholesterol metabolism and heterozygous mutation in sterol 27-hydroxylase gene (CYP27). J.Inherit.Metab.Dis. 24: 379-392
Xanthomatosis, Cerebrotendinous Van BogaertScherer-Epstein Disease; Bogaert-Scherer-Epstein Disease, Van; CerebrotendinousXanthomatoses; cerebrotendinous xanthomatosis; Disease, Van Bogaert http://medical.webends.com/kw/Xanthomatosis, Cerebrotendinous
Extractions: WWW Medical.WebEnds.com Van Bogaert-Scherer-Epstein Disease; Bogaert-Scherer-Epstein Disease, Van; Cerebrotendinous Xanthomatoses; Cerebrotendinous Xanthomatosis; Disease, Van Bogaert-Scherer-Epstein; Van Bogaert Scherer Epstein Disease A lipid storage disease , inherited as an autosomal recessive trait, characterized by xanthomas of the tendons , the white matter of the brain , and the lungs, and by spasticity, ataxia , pyramidal paresis mental retardation dementia , early cataracts, and atherosclerosis. It is associated with elevated plasma and tissue levels of cholestanol and defective bile synthesis, with the deposition of cholestanol in the central nervous system and myelin of peripheral nerves . The lesions contain cholesterol and dehydro cholesterol . (Dorland, 28th ed)
QJMed -- Abstracts: Watts Et Al. 89 (1): 55 Press. ORIGINAL PAPERS. cerebrotendinous xanthomatosis a family studyof sterol 27hydroxylase mutations and pharmacotherapy. GF Watts http://qjmed.oupjournals.org/cgi/content/abstract/89/1/55
Extractions: University Department of Medicine, University of Western Australia, Perth. We examined the phenotypic characteristics, molecular genetics and optimal pharmacological treatment of cerebrotendinous xanthomatosis (CTX) in an English family with combined hyperlipidaemia. The proband presented in adulthood with classical clinical characteristics of CTX, a greater than tenfold elevation in plasma cholestanol and combined hyperlipidaemia. His brother also had typical features of CTX without the presence of dyslipidaemia. Genotyping revealed that the two brothers were compound
Journal Of Internal Medicine Abstract Coronary heart disease in a patient with cerebrotendinous xanthomatosis. Coronaryheart disease in a patient with cerebrotendinous xanthomatosis (Case report). http://blackwellpublishing.com/abstract.asp?ref=0954-6820&vid=255&iid=6&aid=8&s=
