A case of alkaptonuria presenting rapidadvancing hip joint destruction.

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Hip Joint Trevor Disease: Literature Review and a Case Report

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Alkaptonuria: A case report

Alkaptonuria is a rare inborn error of metabolism with autosomal recessive inheritance with a mutation in homogentisate 1,2-dioxygenase. It results in accumulation of homogentisic acid in connective tissues (ochronosis). Most common ocular manifestations are bluish-black discoloration of the conjunctiva, cornea, and sclera. In this case report, a 39-year-old Indian male patient with additional ...

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Ochronosis of hip joint; a case report

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Ochronosis is connective tissue manifestation of Alkaptonuria. Joint involvement especially hip and knee destruction is seen. The cartilage is pigmented and destroyed. A 55years old male (Figure 1) with a previous total arthroplasty on both shoulders, has recently develop a hip pain. He was affected of alkaptonuria (AKU). We proceed with a total hip arthroplasty with cement less cup and modular...

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ژورنال

عنوان ژورنال: Orthopedics & Traumatology

سال: 1987

ISSN: 1349-4333,0037-1033

DOI: 10.5035/nishiseisai.36.508