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         Alkaptonuria:     more detail
  1. Alkaptonuria: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Margaret, PhD Alic, 2005
  2. Alkaptonuria - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19
  3. The Genetic Basis of Alkaptonuria. Contained in Proceedings of the Royal Society of Edinburgh Session 1931-32, Volume 52, Issue 3 pages 264-295. by Lancelot Hogden , 1932-01-01
  4. Skin Conditions Resulting From Errors in Metabolism: Phenylketonuria, Adrenoleukodystrophy, Gout, Porphyria, Lafora Disease, Alkaptonuria

81. UK.SearchEngine.com - Finds It Fast!
alkaptonuria. additional alkaptonuria Categories for alkaptonuria see also/TOP/Health Genetic_Disorders/alkaptonuria other alkaptonuria Sites
http://uk.searchengine.com/Top/Health/Conditions_and_Diseases/Genetic_Disorders/
Home Top Health > Alkaptonuria ADULT CARS SHOPPING FINANCE ...
Alkaptonuria and Ochronosis
- A detailed look at these disorders, how it affects the many body parts, diagnosis, diet and treatment are discussed.
Alkaptonuria
- A brief discussion about this disease and its statistics world wide. Followed by a case study of a 4 year old boy, whose parents noted the darkening of the urine to an almost black color when it was left standing.
MedicineNet.com : Alkaptonuria
- An article about this disease beginning with an explanation as to what it is, followed by how it is inherited, how it affects the joints, symptoms, diagnosis and treatment.
eMedicine Online Text: Alkaptonuria
- An in depth look at this disorder written by Karl S Roth, MD. From a description to treatment all aspects of this disease are discussed.
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82. Mioti: Medical Condition
Condition alkaptonuria. MEDLINEplus alkaptonuria. NORD alkaptonuria. Informationfrom the National Organization for Rare Disorders. OMIM alkaptonuria.
http://www.mioti.com/cat/condition/condition.asp?Cat=Alkaptonuria

83. Birth Disorder Information Directory - A
Alexander('s) Disease/Syndrome List of Sites; Also see Leukodystrophy. alkaptonuria(,Hereditary) (Alkaptonuric Ochronosis, Homogentisic Acid Oxidase Deficiency
http://www.bdid.com/defectag.htm

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84. Mutational Analysis Of The HGO Gene In Finnish Alkaptonuria Patients
P, Luopajärvi K, Matintalo P, Alho A, Konttinen Y, Krohn K, de Cordoba SR, RankiA. Mutational analysis of the HGO gene in Finnish alkaptonuria patients.
http://www.hytti.uku.fi/tays/julkaisut/1999/9900650.html
Julkaisu
Reference
de Bernabe DB, Peterson P, Luopajärvi K, Matintalo P, Alho A, Konttinen Y, Krohn K, de Cordoba SR, Ranki A. Mutational analysis of the HGO gene in Finnish alkaptonuria patients. J Med Genet
Julkaisutiedot
Julkaisutyyppi: Alkuperäisartikkeli.
Kansainvälinen.
Kieli: Englanti.
Teksti/tiivistelmä:
Publication data
Publication type: Original scientific article.
International.
In English.
Text/summary:
Tekijät
Contributors
Tampereen yliopisto

85. Sinisen Miehen Salaisuus: Alkaptonuria
Julkaisu. Reference. VähäKreula T, Luopajärvi K, Peterson P, Kuokkanen K,Ranki A. Sinisen miehen salaisuus alkaptonuria. Duodecim 19971132175-2179.
http://www.hytti.uku.fi/tays/julkaisut/1997/9700188.html
Julkaisu
Reference
Vähä-Kreula T, Luopajärvi K, Peterson P, Kuokkanen K, Ranki A. Sinisen miehen salaisuus: alkaptonuria. Duodecim
Julkaisutiedot
Julkaisutyyppi: Alkuperäisartikkeli.
Kansallinen.
Kieli: Suomi.
Publication data
Publication type: Original scientific article.
National.
In Finnish.
Tekijät
Contributors
Tampereen yliopisto

86. Health Content Encyclopedia Article Alkaptonuria
alkaptonuria is a rare inherited disorder of metabolism characterizedby urine which turns black when exposed to air. alkaptonuria.
http://www.centralbap.com/adamcontent/ency/article/001200.asp

87. Diagnose-Me: Conditions: Ochronosis / Alkaptonuria
Ochronosis / alkaptonuria, Signs, symptoms and indicators, Signs, symptoms indicatorsof Ochronosis / alkaptonuria Symptoms Nails, Blue and brown fingernails.
http://www.diagnose-me.com/cond/C451501.html
Home FAQ Start The Analyst Last updated: Dec 20, 2002
Ochronosis / Alkaptonuria
Signs, symptoms and indicators
Ochronosis is the muscoskeletal manifestation of alkaptonuria - a rather rare (one in 200,000 births) inherited disorder of protein metabolism characterized by an inability of the body to metabolize the amino acids tyrosine and phenylalanine . It affects especially the large joints (hip, knees and vertebral column) by a progressive degenerative arthrosis The outward signs are the ocular (eye) and the skin pigmentations, the genito-urinary calculi (stones) and cardiovascular ochronosis (especially the aortic valve). The symptoms mostly begin within the third or fourth decade.
It was Scribonius who described the first known case of ochronosis in 1584. He mentioned a schoolboy who passed urine black as ink. In 1902, Albrecht and Zdareck discovered the link with alkaptonuria. The incidence of alkaptonuria is 1 per million with the highest prevalence in Slovakia by inbreeding. [ Laoussadi S., Menkes C.-J. Arthroses D’Etiologie rare. Rev. Rhum. Ed. Fr., nr 9 bis, Vol. 61, Nov. 1994
There is no cure for ochronotic arthropathy. The

88. Alkaptonuria
alkaptonuria. A Medical Encyclopedia Maryland Medical System. A resourcewith information on over 4000 medical topics including alkaptonuria.
http://www.bloodandmarrowtransplant.com/medical-terms/03112.htm
Alkaptonuria
A Medical Encyclopedia Article provided by Maryland General Hospital A resource with information on over 4000 medical topics including: Alkaptonuria
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89. Alkaptonuria In Health > Conditions And Diseases > Genetic Disorders
Top categories Support Groups@ (14). Sites alkaptonuria. A brief discussionabout this disease and its statistics world wide. alkaptonuria and Ochronosis.
http://ilectric.com/browse/web/Health/Conditions_and_Diseases/Genetic_Disorders/
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A brief discussion about this disease and its statistics world wide. Followed by a case study of a 4 year old boy, whose parents noted the darkening of the urine to an almost black color when it was left standing.

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