Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.6.1.2 (
alanine aminotransferase
)
26,722
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
A 34-year-old man had asymptomatic hepatomegaly, slightly increased serum
alanine aminotransferase
and gamma-glutamyl transpeptidase levels, and a sonographic pattern suggesting diffuse hepatic steatosis. Liver biopsy revealed fatty change in 25% to 50% of hepatocytes. The patient also had low serum levels of cholesterol and triglycerides and met clinical, biochemical, and familial diagnostic criteria of heterozygous
hypobetalipoproteinemia
. We could not relate his hepatic steatosis to any already known cause of fatty liver and could only attribute it to heterozygous
hypobetalipoproteinemia
. Familial heterozygous
hypobetalipoproteinemia
should be ruled out in patients with unexplained hepatic steatosis.
...
PMID:Diffuse fatty liver in familial heterozygous hypobetalipoproteinemia. 941 28
A 32-year-old man presented with increases in serum
alanine aminotransferase
activity, iron concentration, and transferrin saturation, suggestive of hepatic dysfunction and iron overload. In addition, he had unusually low plasma concentrations of LDL-cholesterol and apolipoprotein (apo) B. Hepatic ultrasonography was consistent with fatty liver. On liver biopsy, marked steatosis and moderate to marked iron deposition were observed. The patient was found to carry the HFE C282Y and H63D mutations, which are associated with hereditary hemochromatosis, and the alpha(1)-antitrypsin PiZ variant. An immunoblot of plasma for apoB showed the presence of a truncated apoB species, indicative of familial
hypobetalipoproteinemia
. DNA sequence analysis revealed that the patient was heterozygous for the apoB-80.5 (c.11040T>G) mutation. This unique case shows an unusual combination of underlying disorders that could all be contributing to liver dysfunction and fatty liver.
...
PMID:Liver dysfunction and steatosis in familial hypobetalipoproteinemia. 1551 99