{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,14]],"date-time":"2026-07-14T04:46:22Z","timestamp":1784004382598,"version":"3.55.0"},"reference-count":19,"publisher":"Termedia Sp. z.o.o.","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Reumatologia"],"published-print":{"date-parts":[[2019,9,24]]},"abstract":"<jats:p>The authors report a female case of systemic lupus erythematosus (SLE) that was diagnosed as Wilson\u2019s disease (WD) when neurological manifestations were evident three years after the first admission. The brain imaging studies showed bilateral symmetrical basal ganglia involvement, slit lamp examination revealed Kayser-Fleischer ring of the cornea, and 24-hour urinary copper and serum ceruloplasmin also confirmed the diagnosis. The patient also had hemolytic anemia and hypoparathyroidism, which are rare presenting features of WD. SLE may be associated with WD, and presence of neurological, behavioral, or liver function abnormalities should raise the suspicion, even without apparent features of WD.<\/jats:p>","DOI":"10.5114\/reum.2019.87622","type":"journal-article","created":{"date-parts":[[2019,9,5]],"date-time":"2019-09-05T10:39:27Z","timestamp":1567679967000},"page":"239-242","source":"Crossref","is-referenced-by-count":7,"title":["Systemic lupus erythematosus, hypoparathyroidism, and hemolytic anemia in a patient with Wilson\u2019s disease"],"prefix":"10.5114","volume":"57","author":[{"given":"Sarah","family":"Mageed","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Prashanth","family":"Rawla","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mariam","family":"Mahmoud","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Abeer","family":"Shahba","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"3061","published-online":{"date-parts":[[2019,8,31]]},"reference":[{"key":"ref-776990","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1038\/ng1293-327","article-title":"The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene","volume":"5","author":"Bull PC","year":"1993","unstructured":"Bull PC, Thomas GR, Rommens JM, et al. (1993). The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene Nat Genet. 5: 327-337.","journal-title":"Nat Genet"},{"key":"ref-776991","doi-asserted-by":"crossref","first-page":"1475","DOI":"10.1053\/jhep.2003.50252","article-title":"A practice guideline on Wilson disease","volume":"37","author":"Roberts EA","year":"2003","unstructured":"Roberts EA, Schilsky ML. (2003). A practice guideline on Wilson disease Hepatology. 37: 1475-1492.","journal-title":"Hepatology"},{"key":"ref-776992","doi-asserted-by":"crossref","first-page":"1725","DOI":"10.1002\/art.1780400928","article-title":"Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus","volume":"40","author":"Hochberg MC","year":"1997","unstructured":"Hochberg MC. (1997). Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus Arthritis Rheum. 40: 1725-1725.","journal-title":"Arthritis Rheum"},{"key":"ref-776993","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1097\/MD.0b013e318045a00e","article-title":"Wilson disease: description of 282 patients evaluated over 3 decades","volume":"86","author":"Taly AB","year":"2007","unstructured":"Taly AB, Meenakshi-Sundaram S, Sinha S, et al. (2007). Wilson disease: description of 282 patients evaluated over 3 decades Medicine (Baltimore). 86: 112-121.","journal-title":"Medicine (Baltimore)"},{"key":"ref-776994","first-page":"4708","article-title":"Hemolytic anemia as first presentation of Wilson\u2019s disease with uncommon ATP7B mutation","volume":"8","author":"Ye X-N","year":"2015","unstructured":"Ye X-N, Mao L-P, Lou Y-J, Tong H-Y. (2015). Hemolytic anemia as first presentation of Wilson\u2019s disease with uncommon ATP7B mutation Int J Clin Exp Med. 8: 4708-4711.","journal-title":"Int J Clin Exp Med"},{"key":"ref-776995","first-page":"55","article-title":"Haemolytic Anaemia as First Manifestation of Wilson\u2019s Disease: A Report of Two Cases","volume":"62","author":"Santra G","year":"2014","unstructured":"Santra G, Rudrajit P, Partha Sarathi Choudhury, et al. (2014). Haemolytic Anaemia as First Manifestation of Wilson\u2019s Disease: A Report of Two Cases J Assoc Physicians India. 62: 55-57.","journal-title":"J Assoc Physicians India"},{"key":"ref-776996","first-page":"81","article-title":"Wilson\u2019s Disease with Systemic Lupus Erythematosus","volume":"64","author":"Santhakumar R","year":"2016","unstructured":"Santhakumar R, Gayathri K, Ramalingam PK, et al. (2016). 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