Portal Toolkit Invalid Site URL Ocular ochronosis A case report and clinical findings. Çakmak, Sevin Söker 1;Çevik, Products of ochronosis may also cause degenerative arthritis. http://ppv.ovid.com/pt/re/acop/fulltext.00043481-200206000-00021.htm
University Of Miami School Of Medicine - Glossary - Alkaptonuria Other causes of ochronosis that mimic alkaptonuria include the prolonged The doctor will suspect alkaptonuria (ochronosis) when the patient reports the http://www.med.miami.edu/glossary/art.asp?articlekey=7804
MedlinePlus Medical Encyclopedia: Alkaptonuria Alcaptonuria; Homogentisic acid oxidase deficiency; ochronosis. Definition Returnto top. Alkaptonuria is a rare inherited disorder of metabolism, http://www.nlm.nih.gov/medlineplus/ency/article/001200.htm
Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Alternative names Alcaptonuria; Homogentisic acid oxidase deficiency; Ochronosis Definition Return to top Alkaptonuria is a rare inherited disorder of metabolism , characterized by urine that turns black when exposed to air. Another characteristic is the development of arthritis in adulthood. Causes, incidence, and risk factors Return to top Alkaptonuria is an autosomal recessive inherited disorder. In affected individuals, an amino acid known as tyrosine is not properly metabolized, due to a defect in an enzyme called homogentisic acid oxidase. Because of the defect, homogentisic acid is excreted in the urine and turns a brown color upon exposure to air. This is the result of a dark pigment with an ochre color (earthy red or yellow), which led to the name ochronosis. The bones and cartilage of the body may be brown-colored. Symptoms Return to top Infant or child: Adult: Progressive arthritis, especially of the spine
Extractions: @import "/css/global.css"; @import "/css/article.css"; ABOUT US ACCESS SUBMISSIONS SUBSCRIBE ... Vol. 16 No. 2 (February 1995) Pp. 285-286 Search Advanced Search Browse by Subject Browse All Stay Informed Select one Basic Research Behavioral and Social Science Issues Cardiology and Cardiovascular Diseases Cardiovascular Surgical Procedures Clinical Research Emergency Cardiovascular Treatment Pediatric and Congenital Heart Disease Preventive Medicine Risk Factors Stroke and Cerebrovascular Disorders Set up email and RSS alerts to keep up-to-date. Issues Editor's choice (free access) Fast track articles Guidelines This Article Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Request Permissions PubMed PubMed Citation Articles by Cortina, R Articles by Cortina, A R Cortina
Extractions: Otto Dornblüth O Ochronosis VIRCHOW, BOSTRÖM gr. ôchros gelblich, nasos Krankheit , schwärzliche Pigmentierung der Grundsubstanz der Knorpel, auch der Sehnen und der Arterienintima, durch Blutfarbstoff, bei chronischer Karbolvergiftung. Der Harn färbt sich bei Luftzutritt, d. h. Aufnahme von Alkali braunschwarz: Alkaptonurie. Ursache Tyrosin, s. d. - Ochropyra gr. pyrh Feuer , Gelbfieber. TO TOP
Ochronosis - Definition Of Ochronosis In Encyclopedia Clinical Manifestations of ochronosisPathognomonic signs of ochronosis were the black deposits in the sclerae The most important clinical signs of ochronosis are the pigmentations of the http://encyclopedia.laborlawtalk.com/ochronosis
Extractions: This article is licensed under the GNU Free Documentation License . It uses material from the Wikipedia article "ochronosis" Browse Ochroma lagopus Ochnaceae ochronosis octadecanoic acid ... octameter Search Word: General Encyclopedia Legal Medical Computer Science Law Forum Embed a dictionary search in your own web page Link to Us Advertise Add to Favorites ...
Alkaptonuria Another characteristic is the development of arthritis in adulthood. AlternativeNames. Alcaptonuria; Homogentisic acid oxidase deficiency; ochronosis http://www.healthscout.com/ency/1/001200.html
Extractions: Search HealthScout Web MEDLINE Special Offers TV Specials Chronic Pain Erectile Dysfunction GERD Diabetes ... High Tech Health Top Features Bipolar Disorder Resources Sleep Skin Cancer Migraines ... Diabetes Health Organizer Resources Healthscout News 3D Health Animations Health Videos Health Encyclopedia ... Drug Library Drug Information Drug Search Drug Interactions Image Database Pill Identifier Channels Home Today Women Men ... Drug Checker Medical Health Encyclopedia Injury Disease Nutrition Poison ... Prevention Definition: Alkaptonuria is a rare inherited disorder of metabolism characterized by urine which turns black when exposed to air. Another characteristic is the development of arthritis in adulthood.
Internet Scientific Publications, LLC. The striking clinical feature of ochronosis is blueblack pigmentation of the Peripheral arthropathy in ochronosis involves large joints, namely, knee, http://www.ispub.com/ostia/index.php?xmlFilePath=journals/ijos/vol2n1/ochronosis
Spine - UserLogin In patients with no other signs of alkaptonuria or ochronosis, early detection Discoloration of the connective tissues, called ochronosis, may vary from http://www.spinejournal.com/pt/re/spine/fulltext.00007632-200008150-00021.htm
Obstetrics & Gynecology -- Sign In Page BACKGROUND ochronosis is a manifestation of alkaptonuria, ochronosis is thesystemic deposition of this pigment, most commonly in the joints, http://www.greenjournal.org/cgi/content/full/101/5/1066
Extractions: This Article Abstract Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Gatcliffe, T. A. Articles by Kasznica, J. To view this item, select one of the options below: Sign In User Name Sign in without cookies.
Alkaptonuria Alcaptonuria; Homogentisic acid oxidase deficiency; ochronosis pigment withan ochre color (earthy red or yellow), which led to the name ochronosis. http://www.shands.org/health/information/article/001200.htm
Extractions: Causes, incidence, and risk factors: Alkaptonuria is an autosomal recessive inherited disorder. In affected individuals, an amino acid known as tyrosine is not properly metabolized, due to a defect in an enzyme called homogentisic acid oxidase. Because of the defect, homogentisic acid is excreted in the urine and turns a brown color upon exposure to air. This is the result of a dark pigment with an ochre color (earthy red or yellow), which led to the name ochronosis. The bones and cartilage of the body can be brown colored.
Clinical Orthopaedics And Related Research - UserLogin Bilateral Achilles Tendon Ruptures in a Patient With ochronosis A Case Report We report the case of a 67year-old man with ochronosis who had bilateral http://www.corronline.com/pt/re/corr/fulltext.00003086-200407000-00027.htm
Ochronosis We thank you for using the Health Dictionary to search for ochronosis. If youhave a better definition for ochronosis than the one presented here, http://www.healthdictionary.info/Ochronosis.htm
Extractions: Search : Log in Ochronosis See 'Alkaptonuria'. In case you consider this not informative enough please send us your suggestion We thank you for using the Health Dictionary to search for Ochronosis. If you have a better definition for Ochronosis than the one presented here, please let us know by making use of the suggest a term option above. This definition of Ochronosis may be disputed by other professionals. Our attempt is to provide easy definitions on Ochronosis and any other medical topic for the public at large.
Www.rikai.com/wordmap/ochronosis%23n%251 Disease Alkaptonuria - Detroit, MichiganAlcaptonuria; Homogentisic acid oxidase deficiency; ochronosis. Causes And Risk.Alkaptonuria is an autosomal recessive inherited disorder. http://www.rikai.com/wordmap/ochronosis#n%1
Extractions: Clinical form to enter cases in a alkaptonuria/ochronosis database Please, fill as many fields as possible. All data will be strictly confidential (*). Name (first three letters) Surname (first three letters) Sex F M Birth Date (dd/mm/yy) Age at the present visit Mother's origin (specify the geographic area) Mother's ethnic group Father's origin (specify the geographic area) Father's ethnic group Consanguineity between mother and father YES NO If YES, specify Number brothers/sisters To exclude the presence of the metabolic defect in the other sibs, please, perform the fast test to detect the presence of homogentisic acid in the urine: add to a urine sample some drops of NaOH 1M. Test is positive if the color of the urine turns brown-black. If the fast test is positive in brothers/sisters, please fill another form. Assay of homogentisic acid in the urine (specify methods and units used) Are you willing to send biological material ? YES NO CLINICAL FINDINGS Pigment deposition auricles YES NO nails YES NO sclerae YES NO skin YES NO Other (specify): Valvular heart disease aortic YES NO mitralic YES NO Genito-urinary calculi bladder YES NO prostate YES NO Ipoacusia YES NO Ochronotic Arthropathy If present, please fill in the following part:
ALKAPTONURIA: CASE REPORT AND REVIEW OF THE LITERATURE ochronosis report of a case. Ann Intern Med 1957;46179. Sickert RG, Gibilisco JA.Discoloration of the teeth in alkaptonuria (ochronosis) and Parkinsonism http://www.kfshrc.edu.sa/annals/185/98-055.html
Extractions: ALKAPTONURIA: CASE REPORT AND REVIEW OF THE LITERATURE M. Al-Essa, MD; L. Al-Shamsan; M.S. Rashed, PhD ; P.T. Ozand, MD PhD Alkaptonuria (McKusick 203500) is a rare metabolic disease characterized by a triad of homogentisic aciduria, arthritis and ochronosis. It enjoys the historic distinction of being one of the first conditions in which mendelian recessive inheritance was proposed and is also one of the conditions in the charter of group of inborn errors of metabolism. It is of interest to note that the disease was identified in 1500 BC in an ancient egyptian mummy. The manifestations are urine that turns dark on standing and alkalinization due to excretion of excessive amounts of homogentisic acid, large joint arthritis and black ochronotic pigmentation of cartilage and collagenous tissue. This disease is unusually frequent in Slovakia and the Dominican Republic. More than 126 patients have been reported from Czechoslovakia, 108 from Germany, and 90 from the United States. In countries of the Middle East, the disease was first reported from Lebanon in 1958 and from Sudan in 1965.
All Showcase - Ochronosis Case Number 29 ochronosis synovial histopathological ochronosis is a rare autosomal recessive disorder featuring total lack of the enzyme Schumacher H. ochronosis, hemochromatosis, and Wilsons disease. http://www.allshowcase.com/Health_and_Fitness/Conditions_and_Diseases/O/Ochronos
Extractions: Vol Page [Advanced] This Article Full Text Full Text (PDF) Submit a response ... Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Kruithof, E Articles by Verdonk, R Related Collections Other Rheumatology Annals of the Rheumatic Diseases E Kruithof D Baeten E M Veys F De Keyser S Suykens L De Wilde and R Verdonk Series editor: Gary D Wright Department of Rheumatology, Ghent University Hospital, Belgium
