Hip and knee replacement in patients with ochronosis: Clinical experience and literature review
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چکیده
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the past hospitalization and its association with suicide attempts and ideation in patients with mdd and comparison with bmd (depressed type) group
چکیده ندارد.
Ochronosis - The Role of Total Hip Replacement : A Case Report and Review of Literature
Alkaptonuria is a rare autosomal recessive, single-gene metabolic disease caused by the lack of the enzyme homogentisic acid oxidase and characterized by black pigmentation of cartilage and other connective tissues. 38 yr old male was admitted to the orthopedics ward with bilateral hip pain for the past 3 years and inability to walk for the past 1yr. He had also complained of brownish-black dis...
متن کاملKnee and Hip Joint Replacement Surgery in a Patient with Ochronotic Arthropathy: Surgical Tips
Ochronosis or black joints disorder is a rare autosomal recessive disorder caused by deficiency of homogentisic acidoxidase. Orthopaedic manifestations are common and mostly involve spine and large joints such as knee and hip.Arthropathy is progressive and will eventually leads to arthroplasty. Not being familiar with this disorder might lead todevastating complications. We present a 57 year-ol...
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این پایان نامه به بررسی بومی سازی و بیگانه سازی در ادبیات کودکان مخصوصا زانر فانتزی می پردازد. در این پایان نامه ترجمه 14 کتاب داستان فانتزی برای سه گروه سنی کودکان بر اساس مدل ونوتی یعنی بومی سازی و بیگانه سازی مقاسه شدندکه در نتیجه برای سه گروه سنی از هر دو استراتزی توسط مترجمان در ترجمه کلمات فرهنگی استفاده شده است.
Hip and knee replacement.
OBJECTIVES This article examines trends in hip and knee replacement surgery between 1981/82 and 1998/99, focussing on procedures involving seniors. It also presents 1998/99 data on readmissions within 30 days. DATA SOURCES Data on hip and knee replacement are from the Hospital Morbidity Database for 1981/82 through 1998/99. The Person-oriented Information Database is used to examine readmissi...
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ژورنال
عنوان ژورنال: Orthopedic Reviews
سال: 2020
ISSN: 2035-8164,2035-8237
DOI: 10.4081/or.2020.8687