A Case Report of Shoulder Arthropathy due to Alkaptonuria.
نویسندگان
چکیده
منابع مشابه
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 ...
متن کاملAlkaptonuria - Case report*
Alkaptonuria, also called endogenous ochronosis, is a rare metabolic autosomal recessive disorder. It occurs by complete inhibition of homogentisic acid oxidase enzyme having its deposition in various tissues. Male patient, 52 years old, sought medical help complaining about progressive appearance of hyperchromic papules on the lateral edge of the second finger of both hands for 02 years. He al...
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ژورنال
عنوان ژورنال: Orthopedics & Traumatology
سال: 2002
ISSN: 1349-4333,0037-1033
DOI: 10.5035/nishiseisai.51.450