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Information Journal Paper

Title

A CASE REPORT ON ALKAPFONURIA

Pages

  87-89

Abstract

 Alkaptonuria is a very rare hereditary disease with the liver enzyme homogentisic oxidase deficiency which is the result of accumulation of HOMOGENTISIC ACID in tissues along with excretion in urine in large quantities. Ochronosis is clinical expression of alkaptonuria with the symptoms on the visceral organ, articular and connective tissues. The patient was a middle-aged man with prolong pain and stiffness of the left shoulder and knee. Urine discolouration war noticed. Articular biopsy and urine screening test were done. as confirmatory diagnostic tests.

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  • Cite

    APA: Copy

    TORABIZADEH, ZH., NAGHSHVAR, F., & EMADIAN, O.. (2001). A CASE REPORT ON ALKAPFONURIA. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 11(31), 87-89. SID. https://sid.ir/paper/46097/en

    Vancouver: Copy

    TORABIZADEH ZH., NAGHSHVAR F., EMADIAN O.. A CASE REPORT ON ALKAPFONURIA. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2001;11(31):87-89. Available from: https://sid.ir/paper/46097/en

    IEEE: Copy

    ZH. TORABIZADEH, F. NAGHSHVAR, and O. EMADIAN, “A CASE REPORT ON ALKAPFONURIA,” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 11, no. 31, pp. 87–89, 2001, [Online]. Available: https://sid.ir/paper/46097/en

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