Literature DB >> 20229718

Alkaptonuria.

Anida Grosicka1, Eugeniusz Józef Kucharz.   

Abstract

Alkaptonuria is a hereditary disease resulted from accumulation of homogentisic acid within the body due to deficiency of homogentisic acid oxidase. The main clinical feature is dark brown color of urine caused by high urinary output of homogentisic acid. There are no other symptoms or signs of the disease until the fourth decade of life when ochronosis is developed. Life-long accumulation of abnormal metabolites becomes overt in form of severe spondylosis, peripheral arthropathy, tendon rupture, bone osteoporosis as well as aortic valve stenosis and skin pigmentation. The features of the disease are associated with affinity of homogentisic acid to the connective tissue and its effect on collagen structure. Only symptomatic treatment is applied in case of alkaptonuria and ochronosis.

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Year:  2009        PMID: 20229718

Source DB:  PubMed          Journal:  Wiad Lek        ISSN: 0043-5147


  3 in total

1.  Subchondral insufficiency fracture of the femoral head in a patient with alkaptonuria.

Authors:  Takahiro Hamada; Takuaki Yamamoto; Jun-ichi Shida; Akihiko Inokuchi; Takeshi Arizono
Journal:  Skeletal Radiol       Date:  2013-12-20       Impact factor: 2.199

2.  Spontaneous Achilles tendon rupture in alkaptonuria.

Authors:  Omar A Alajoulin; Mohammed S Alsbou; Somayya O Ja'afreh; Heba M Kalbouneh
Journal:  Saudi Med J       Date:  2015-12       Impact factor: 1.484

3.  Neurological Assessment and Nerve Conduction Study Findings in 22 Patients with Alkaptonuria from Jordan.

Authors:  Omar Alrawashdeh; Mohammad Alsbou; Hamed Alzoubi; Hani Al-Shagahin
Journal:  Neurol Int       Date:  2017-01-05
  3 in total

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