Literature DB >> 24286097

A case of alkaptonuria - ultrasonographic findings.

Laura Otilia Damian1, Ioana Felea, Călin Boloşiu, Carolina Botar-Jid, Daniela Fodor, Simona Rednic.   

Abstract

Alkaptonuria is a rare disease with autosomal recessive inheritance and variable expression. The weight-bearing joint involvement and spondylitis-like vertebral changes occur only after the 3rd decade. Musculoskeletal ultrasonographic findings in alkaptonuria were only rarely described, consisting mainly into enthesopathy and non-synovial tendon degeneration. We present the case of a 50 years old man with alkaptonuria and discuss the ultrasonographic findings and the relationship of the disease with chondrocalcinosis. The tendinous and synovial aspect may be peculiar and it could therefore allow recognition and screening for alkaptonuria, along with clinical and radiologic data.

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Year:  2013        PMID: 24286097     DOI: 10.11152/mu.2013.2066.154.lod2

Source DB:  PubMed          Journal:  Med Ultrason        ISSN: 1844-4172            Impact factor:   1.611


  2 in total

1.  Alkaptonuria.

Authors:  Manish Thapa; M Bhatia; V K Maurya
Journal:  Med J Armed Forces India       Date:  2017-07-25

2.  Cartilage biomarkers in the osteoarthropathy of alkaptonuria reveal low turnover and accelerated ageing.

Authors:  Adam M Taylor; Ming-Feng Hsueh; Lakshminarayan R Ranganath; James A Gallagher; Jane P Dillon; Janet L Huebner; Jon B Catterall; Virginia B Kraus
Journal:  Rheumatology (Oxford)       Date:  2016-10-07       Impact factor: 7.580

  2 in total

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