Results 91 to 100 of about 2,772 (216)
Clinical features and outcome in patients with osseomuscular type of Wilson’s disease [PDF]
BACKGROUND: Wilson's disease with osseomuscular type is a rare condition, which often lacks typical hepatic and neurological symptoms and causes misdiagnoses easily.
Hao Yu +6 more
core +1 more source
The metabolic balances of sulfur in two cases of hepatolenticular degeneration were studied. A positive balance was found in both cases; in one patient submitted to mixed diet, the average was significantly higher than the normal mean. The administration
Horacio M. Canelas +2 more
doaj
Spasmodic Muscle Cramps and Wilson Disease
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
Mismanagement of Wilson′s disease as psychotic disorder
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
Metal Contamination In Commercially Important Fish And Shrimp Species Collected From Aceh (Indonesia), Penang And Perak (Malaysia) [PDF]
Kajian ini dijalankan untuk mengkaji kontaminasi empat logam berat dalam tisu ikan dan udang yang bernilai komersial yang diperolehi dari Aceh (Indonesia) This study was conducted to investigate the contamination of four heavy metals in the tissues of
Sofia, Sofia
core
A Case of Colonic Adenocarcinoma in a Patient with Wilson's Disease
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
Choreiform Wilson's disease and a distinctive 7-Tesla magnetic resonance imaging finding
Chorea is a rare manifestation of Wilson's disease (WD), resulting from copper-induced dysfunction of the basal ganglia. We herein report the case of a 22-year-old woman with progressive dysarthria and generalized chorea, later confirmed as WD.
Ana Rosa Santana +7 more
doaj +1 more source
[Factors influencing the clinical phenotype of hepatolenticular degeneration]. [PDF]
Xiao QQ, Wang ZX, Fan JG.
europepmc +1 more source
A case report on neurological Wilson disease in an adolescent boy [PDF]
Wilson disease is an inherited metabolic multi-system disease that affects primarily the liver and brain. The cirrhotic liver combined with degenerative changes in lenticular nuclei of brain gives it the name of hepatolenticular degeneration.
Anurag +4 more
core +2 more sources
Pregnancy with Wilson’s disease [PDF]
Wilson’s disease is a rare, autosomal recessive disorder characterized by impaired liver metabolism of copper, leading to decreased biliary excretion and incorporation of ceruloplasmin levels mainly in the liver and brain.
Devraj, Nandeesha Thindlu +2 more
core +2 more sources

