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23 Possible Causes for Diffuse Hepatic Steatosis, Hypoglycemia, Wilson Disease

  • Liver Cirrhosis

    Cardinal symptoms include fasting hypoglycemia, lactic acidosis and hepatomegaly as well as neutropenia.[ncbi.nlm.nih.gov] Wilson disease Polycystic liver disease Alpha-1 antitrypsin deficiency Cystic fibrosis Autoimmune Autoimmune hepatitis Biliary cirrhosis Many causes of chronic injury to[symptoma.com] First, perfusion, iron overload, hepatic steatosis, liver inflammation and edema can confound the interpretation of diffusion parameters. 54 Second, DWI is sensitive to motion-related[dx.doi.org]

  • Fatty Liver

    , Spain. cgutierrezj@telefonica.net Abstract Here we report a 7-month-old girl with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency with hypoketotic hypoglycemia[ncbi.nlm.nih.gov] […] hepatic steatosis Wilson disease hepatic fatty infiltration diffuse hepatic steatosis focal hepatic steatosis Promoted articles (advertising)[radiopaedia.org] Hypoglycemia is considered a very important feature in this rare disorder and should help in deciding the diagnosis in an appropriate setting, but there was no hypoglycemia[sjmms.net]

  • Toxic Hepatitis

    Liver cancer Inherited diseases, such as hemochromatosis and Wilson disease Symptoms of liver disease can vary, but they often include swelling of the abdomen and legs, bruising[icdlist.com] diffusely decreased parenchymal attenuation on noncontrast CT diffuse edematous change hepatic steatosis may be a cause (steatohepatitis) or a result of acute hepatitis possible[radiopaedia.org] About Wilson's Disease. Wilson's Disease Association [On-line information]. Available online at . ( 2005) Wilson Disease Screening Panel, Serum.[labtestsonline.org]

  • Macronodular Cirrhosis

    Continued fluid and electrolyte imbalances and inefficient metabolism of nutrients produce ascites, hypoglycemia, and hypoproteinemia.[medical-dictionary.thefreedictionary.com] Elevated serum copper, decreased serum ceruloplasmin, and elevated 24-hours urine may be diagnostic of Wilson’s disease. 14.[encyclopedia.lubopitko-bg.com] On CT, an objective measurement using Hounsfield units of 48 on a noncontrast study is most accurate in diagnosing hepatic steatosis.[jaocr.org]

  • Chronic Liver Disease

    Nocturnal hypoglycemia was seen in 22% of patients.[ncbi.nlm.nih.gov] A detailed discussion of the contraceptive options for patients with chronic liver disease, in general, and Wilson's disease, in particular, follows the case report.[ncbi.nlm.nih.gov] Cutoff values for grading steatosis varied across studies included in the meta-analysis but were not less than 25 % for moderate to severe hepatic steatosis.[link.springer.com]

  • Citrullinemia Type 2

    Hypoglycemia and hypergalactosemia have also been reported as possible features of neonatal-onset CTLN2.[symptoma.com] Exclusive programs under the collaboration will address citrullinemia type 1, phenylketonuria (PKU), and Wilson disease, rare diseases which often have devastating outcomes[oneinfiftyseventhousand.com] Some previous studies [19,35,36] indicated that NICCD patients’ liver biopsies showed varying degrees of hepatic steatosis, diffuse hepatocyte microbubble degeneration, or[journals.lww.com]

  • Hepatitis

    diffusely decreased parenchymal attenuation on noncontrast CT diffuse edematous change hepatic steatosis may be a cause (steatohepatitis) or a result of acute hepatitis possible[radiopaedia.org] Despite advances in intensive care management, mortality continues to be high (40–80%) and is partly related to ALF's complications, such as cerebral edema, sepsis, hypoglycemia[doi.org] About Wilson's Disease. Wilson's Disease Association [On-line information]. Available online at . ( 2005) Wilson Disease Screening Panel, Serum.[labtestsonline.org]

  • Mitochondrial Complex 3 Deficiency

    CC MC3DN9 clinical features include feeding difficulties, CC hypoglycemia, severe lactic acidosis, and delayed psychomotor CC development. {ECO:0000269 PubMed:25008109}.[genome.jp] disease;Hepatolenticular degeneration 1 ORPHA905 E83.0 277900 Menkes disease 1 ORPHA565 E83.0 309400 CYSTIC FIBROSIS 9 ORPHA586 E84 219700 Alpha-1-antitrypsin deficiency[catalogue.rd-connect.eu] hepatic steatosis Poor suck Hepatic failure Rigidity Drooling Aggressive behavior Clonus Retinal degeneration Chorea Spastic tetraplegia X-linked dominant inheritance Athetosis[mendelian.co]

  • Chronic Hepatitis

    Despite advances in intensive care management, mortality continues to be high (40–80%) and is partly related to ALF's complications, such as cerebral edema, sepsis, hypoglycemia[doi.org] These include viral serology, autoantibodies, alpha-1-antitrypsin levels, immunoglobulins, ceruloplasmin levels (in children to rule out Wilson's disease).[symptoma.com] “bright liver” and with deep attenuation; and (3) “severe steatosis”, presence of diffusely severe “bright liver” and deep attenuation without visibility of the diaphragm[doi.org]

  • Mauriac's Syndrome

    The records revealed fluctuating and poorly controlled sugar levels, especially with multiple episodes of hypoglycemia.[jomrjournal.org] Liver cancer Inherited diseases, such as hemochromatosis and Wilson disease Symptoms of liver disease can vary, but they often include swelling of the abdomen and legs, bruising[icdlist.com] Liver biopsy was performed, which revealed findings consistent with diffuse hepatocellular glycogen accumulation. There was no steatosis, fibrosis or inflammation.[ijcasereportsandimages.com]

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