Big Lottery to fund scientific research
...00,000 to develop a treatment for the rare, genetic disease Alkaptonuria.
Patients being treated for the disorder do not have enough of the enzyme, homogentisic
acid oxidase, which causes acid to build up in the body. Some of this acid is eliminated in the urine, but the remainder is deposited in body tissue w...
... ... National Organization for Rare Disorders is dedicated to helping people with rare, ... Alkaptonuria is a rare hereditary disorder in which homogentisic
acid ... Alkaptonuria is a rare condition in which a person's urine turns a dark brownish ... Coronary artery disease may develop earlie...
Homogentisic acid - Wikipedia, the free encyclopedia Homogentisic
acid is the common name for 2,5-dihydroxyphenylacetic acid. ... 4-Hydroxyphenylpyruvic acid · Homogentisic
acid · 4-Maleylacetoacetate. Goxaloacetate ...
homogentisic acid - definition of homogentisic acid by the Free Online ...homogentisic
acid synonyms, homogentisic
acid antonyms. Information about homogentisic
acid - an acid formed as an intermediate product of ...
Homogentisic acid oxidase deficiency
Because of the defect, homogentisic
acid is excreted in the urine and turns a ... Homogentisic
acid products can accumulate on the heart valves, especially the ...
Alkaptonuria | Health Library | Walgreens
Alkaptonuria ... As a result, a substance called homogentisic
acid builds up in the skin and other ... Homogentisic
acid also can build up on the heart valves, especially the ...
Homogentisic acid oxydase deficiency - WrongDiagnosis.comHomogentisic
acid oxydase deficiency symptoms, causes, diagnosis, and treatment ... list of 31 symptoms of Homogentisic
acid oxydase deficiency (Alkaptonuria) ...
Homogentisic acid oxidase deficiency - WrongDiagnosis.comHomogentisic
acid oxidase deficiency symptoms, causes, diagnosis, and treatment ... list of 31 symptoms of Homogentisic
acid oxidase deficiency (Alkaptonuria) ...