Results 81 to 90 of about 177,432 (192)
Anemia following zinc treatment for Wilson’s disease: a case report and literature review
BMC Gastroenterology, 2019 Background Zinc therapy is considered an effective and safe treatment for Wilson’s disease. Hypocupremia-related anemia is rarely reported after long-term zinc administration or combination therapy with copper-chelating agent. Case presentation We herein
Sha Cai +3 more
doaj +1 more source
Spasmodic Muscle Cramps and Wilson Disease
Pediatric Neurology Briefs, 2013 Investigators at Ann & Robert H. Lurie Children's Hospital of Chicago report a case of Wilson disease (WD) in a 10-year-old-boy presenting with 3 months of increasingly severe spasmodic muscle cramps and weakness in lower extremities, upper extremities ...
J Gordon Millichap
doaj +1 more source
Wilson’s Disease. Onset and Complex Diagnosis: Clinical Case
Вопросы современной педиатрииBackground. The low prevalence of Wilson’s disease, diversity of clinical signs, long latent course, inheritance features make it difficult to diagnose and require multidisciplinary approach from doctors. Clinical case description. This article describes
Elena S. Zastelo +4 more
doaj +1 more source
Wilson disease associated with mesangiocapillary glomerulonephritis. A Case Report
, 2007 Wilson`s disease (hepatolenticular degeneration) is an autosomal recessive dis or der of copper transport. It is characterized by the accumulation of copper in the liver and subsequently other organs, mainly the central nervous system and the kidneys ...
Boyadjieva, S.; St. Marina University Hospital of Varna +7 more
core +1 more source
Ultrasound approach to the Wilson’s disease [PDF]
, 2017 Wilson disease (WD) is an autosomal recessive disorder of copper transport which map to chromosome 13q14.3, characterized by the toxic accumulation of copper in a number of organs, particularly the liver and brain [1,2]. Named after the Samuel Kinnear
Sotiroski, Kosta +9 more
core +1 more source
Wilson’s disease: A case report with review of literature [PDF]
, 1970 Wilson’s disease is a rare inborn error of metabolism characterized by abnormal deposition of copper in various tissues caused by the inability to excrete copper into the bile. Wilson’s disease is also known as hepatolenticular degeneration because liver
Rao, Bhimeswara +2 more
core +1 more source
Mismanagement of Wilson′s disease as psychotic disorder
Advanced Biomedical Research, 2012 Wilson′s disease (WD) or hepatolenticular degeneration is an inherited neurodegenerative disorder of copper metabolism (autosomal recessive, chromosome13). Psychiatric disorders in WD include dementia, characterized by mental slowness, poor concentration,
Reza Bidaki +6 more
doaj +1 more source
Walsh & Hoyt: Wilson\u27s Disease
, 2005 Wilsons disease (WD) (hepatolenticular degeneration, Westphal-Strumpell disease) is a genetic disorder of autosomal-recessive inheritance, in which a dysfunction of copper metabolism leads to excessive accumulation of copper, particularly in the liver ...
Parashkev Nachev, PhD, MRCP(UK); Christopher Kennard, PhD, FRCP, FMed Sci
core
A Case of Colonic Adenocarcinoma in a Patient with Wilson's Disease
Gut and Liver, 2013 Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism that results in the accumulation of copper in the body and primarily in the liver, brain, and cornea.
doaj +1 more source
Frequency of LSM failure according to different diseases.
, 2014 LSM failure rate in 38,464 LSM examinations is overviewed (A), and Chi-square test is applied to find the unsuccessful and unreliable LSM rate differences between each disease group and the total failure rate (B).
Dong Ji (615506) +9 more
core +1 more source