BIOMAT Database Logo BIOMAT Database Logo

Hemolysis, coagulation defects, and fulminant hepatic failure as a presentation of Wilson's disease. 1979

E J Doering, and R A Savage, and T E Dittmer

UI MeSH Term Description Entries
D001778 Blood Coagulation Disorders Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATION PROTEIN DISORDERS; BLOOD PLATELET DISORDERS; BLOOD PROTEIN DISORDERS or nutritional conditions. Coagulation Disorders, Blood,Disorders, Blood Coagulation,Blood Coagulation Disorder,Coagulation Disorder, Blood,Disorder, Blood Coagulation
D005260 Female Females
D006505 Hepatitis INFLAMMATION of the LIVER. Hepatitides
D006527 Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. Cerebral Pseudosclerosis,Neurohepatic Degeneration,Pseudosclerosis,Wilson Disease,Copper Storage Disease,Hepatic Form of Wilson Disease,Hepato-Neurologic Wilson Disease,Hepatocerebral Degeneration,Hepatolenticular Degeneration Syndrome,Kinnier-Wilson Disease,Progressive Lenticular Degeneration,Westphal-Strumpell Syndrome,Wilson Disease, Hepatic Form,Wilson's Disease,Cerebral Pseudoscleroses,Copper Storage Diseases,Degeneration Syndrome, Hepatolenticular,Degeneration Syndromes, Hepatolenticular,Degeneration, Hepatocerebral,Degeneration, Hepatolenticular,Degeneration, Neurohepatic,Degeneration, Progressive Lenticular,Degenerations, Hepatocerebral,Degenerations, Neurohepatic,Disease, Copper Storage,Diseases, Copper Storage,Diseases, Hepato-Neurologic Wilson,Diseases, Kinnier-Wilson,Hepato Neurologic Wilson Disease,Hepato-Neurologic Wilson Diseases,Hepatocerebral Degenerations,Hepatolenticular Degeneration Syndromes,Kinnier Wilson Disease,Kinnier-Wilson Diseases,Lenticular Degeneration, Progressive,Neurohepatic Degenerations,Pseudoscleroses, Cerebral,Pseudosclerosis, Cerebral,Storage Disease, Copper,Storage Diseases, Copper,Syndrome, Hepatolenticular Degeneration,Syndromes, Hepatolenticular Degeneration,Westphal Strumpell Syndrome,Westphal-Strumpell Syndromes,Wilson Disease, Hepato-Neurologic,Wilson Diseases, Hepato-Neurologic,Wilsons Disease
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000743 Anemia, Hemolytic A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES). Anemia, Hemolytic, Acquired,Anemia, Microangiopathic,Haemolytic Anaemia,Hemolytic Anemia,Hemolytic Anemia, Acquired,Microangiopathic Hemolytic Anemia,Acquired Hemolytic Anemia,Anaemia, Haemolytic,Anemia, Acquired Hemolytic,Anemia, Microangiopathic Hemolytic,Haemolytic Anaemias,Hemolytic Anemia, Microangiopathic,Microangiopathic Anemia,Microangiopathic Hemolytic Anemias

Related Publications

E J Doering, and R A Savage, and T E Dittmer
Wilson's disease presenting as acute fulminant hepatic failure.
August 1990, Scottish medical journal,
E J Doering, and R A Savage, and T E Dittmer
Diagnosis of Wilson's disease presenting as fulminant hepatic failure.
January 1983, Gastroenterology,
E J Doering, and R A Savage, and T E Dittmer
Fulminant hepatic and renal failure complicating Wilson's disease.
December 1984, Liver,
E J Doering, and R A Savage, and T E Dittmer
Unmeasurable serum alkaline phosphatase activity in Wilson's disease associated with fulminant hepatic failure and hemolysis.
January 1987, Hepatology (Baltimore, Md.),
E J Doering, and R A Savage, and T E Dittmer
[Fulminant hepatitis and acute hemolysis as the symptoms of Wilson's disease].
April 1986, Polski tygodnik lekarski (Warsaw, Poland : 1960),
E J Doering, and R A Savage, and T E Dittmer
Hepatic morphology and histochemistry of Wilson's disease presenting as fulminant hepatic failure: a study of 11 cases.
October 1989, Histopathology,
E J Doering, and R A Savage, and T E Dittmer
Fulminant hepatitis. A presentation of Wilson's disease.
August 1977, American journal of diseases of children (1960),
E J Doering, and R A Savage, and T E Dittmer
[Diagnostic characteristics of acute hepatic failure in fulminant Wilson's disease].
February 1992, Zeitschrift fur Gastroenterologie,
E J Doering, and R A Savage, and T E Dittmer
Fulminant hepatic failure resulting from coexistent Wilson's disease and hepatitis E.
June 1994, Gut,
E J Doering, and R A Savage, and T E Dittmer
A heartbreaking case of Wilson's disease: Takotsubo cardiomyopathy complicating fulminant hepatic failure.
November 2014, Transplant international : official journal of the European Society for Organ Transplantation,
Copied contents to your clipboard!