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2,107 Possible Causes for Albumin Decreased, Cholelithiasis, Mutation in the CDK6 Gene

  • Liver Cirrhosis

    When liver function decreases, the value of albumin also decreases.[otsuka.co.jp] Increasing Child score, INR and decreasing albumin were correlated with TO. In addition, decompensated patients with ascites showed more abnormal TO and TS.[ncbi.nlm.nih.gov] Thus, there is a frequent lack of BCAAs in LC patients, resulting in decreased albumin synthesis.[wjgnet.com]

    Missing: Mutation in the CDK6 Gene
  • Portal Cirrhosis

    […] platelets Splenomegaly Reduced hepatic production of thrombopoietin Direct toxic effect of alcohol on the bone marrow Albumin Decreased in advanced cirrhosis Decreased hepatic[pathophys.org] Such chronic gastrointestinal diseases as peptic ulcer, cirrhosis, and cholelithiasis are becoming increasingly recognized as health problems.[books.google.com] CHOLELITHIASIS 39. TREATMENT CHART 40.[slideshare.net]

    Missing: Mutation in the CDK6 Gene
  • Macronodular Cirrhosis

    : decreased in chronic liver diseases. prothrombin time: increased in acute and chronic liver diseases.[quizlet.com] Cholelithiasis Cholera Cholera Cholestasis Cholestasis Cholesterolosis Cholesterolosis Cirrhosis hepatis biliaris Biliary cirrhosis Cirrhosis hepatis cardialis Cardiac cirrhosis[dentisty.org] Protein metabolism tests show decreased total protein, decreased albumin, and increased globulin.[medical-dictionary.thefreedictionary.com]

    Missing: Mutation in the CDK6 Gene
  • Inflammatory Bowel Disease Type 1

    As seen in Table 4, improvements in hemoglobin (Hgb), white blood cell count, erythrocyte sedimentation rate, and albumin were observed during the course of the study and[journals.lww.com] Probably cholelithiasis is caused by bile salt pool alteration for malabsorption.[doi.org] During the 12-week initial period, HBI decreased from 3.3 2.0 to 0.6 1.3 ( P 0.007) and the PCDAI declined from 21.1 5.9 to 7.8 7.1 ( P 0.011), whereas the LS dropped from[journals.lww.com]

    Missing: Mutation in the CDK6 Gene
  • Primary Biliary Cirrhosis

    albumin levels in the body Easy bruising or bleeding: The liver is responsible for producing blood clotting factors.[medicinenet.com] Associations cholelithiasis ( 40%) 8 other autoimmune diseases, e.g.[radiopaedia.org] Surgical Care As the disease progresses to cirrhosis, an elevated bilirubin level, a prolonged prothrombin time, and a decreased albumin level can be found.[emedicine.medscape.com]

    Missing: Mutation in the CDK6 Gene
  • Ulcerative Colitis

    […] tachycardia syndrome Digestive : peptic ulcer, lactose intolerance, celiac disease, food allergies Glands Bile system Inflammatory: cholecystitis, cholangitis Obstruction: cholelithiasis[en.wikipedia.org]

    Missing: Mutation in the CDK6 Gene
  • Short Bowel Syndrome

    The incidence of cholelithiasis can be minimized by providing enteric nutrition whenever feasible.[dx.doi.org] Limketkai Cholelithiasis and Nephrolithiasis Andrew Ukleja and John Rivas Metabolic Bone Disease in Adults with Short Bowel Syndrome Lynn R. Mack and Fedja A.[routledge.com] Cholelithiasis 36.   Increase risk in colon preserved patients  Binding of non absorbed FFA with calcium releases free oxalate which are soluble and absorbed in colon [slideshare.net]

    Missing: Mutation in the CDK6 Gene
  • Cystic Fibrosis

    […] replacement of pancreas pancreatitis ( acute and chronic ) pancreatic cysts liver hepatic steatosis focal biliary and multilobular cirrhosis portal hypertension biliary system cholelithiasis[radiopaedia.org] […] obstruction syndrome Rectal prolapse Vitamin deficiency (especially fat-soluble vitamins) Fatty liver Focal biliary cirrhosis Portal hypertension Liver failure Cholecystitis and cholelithiasis[emedicine.medscape.com] There is an increased incidence of cholelithiasis, which is usually asymptomatic.[merckmanuals.com]

    Missing: Mutation in the CDK6 Gene
  • Progressive Familial Intrahepatic Cholestasis

    Two siblings presented, before the age of 30 years, recurrent symptomatic cholelithiasis and extensive biliary fibrosis that progressed towards portal hypertension and liver[ncbi.nlm.nih.gov] High serum alanine aminotransferase and alphafetoprotein levels, severe lobular lesions with giant hepatocytes, early liver failure, cholelithiasis, hepatocellular carcinoma[ncbi.nlm.nih.gov] Rosmorduc O, Hermelin B, Poupon R : MDR3 gene defect in adults with symptomatic intrahepatic and gallbladder cholesterol cholelithiasis.[nature.com]

    Missing: Mutation in the CDK6 Gene
  • Cardiac Cirrhosis

    albumin and globulin, prothrombin time prolonged, the latter can not be corrected with vitamin K, and with the improvement of congestive heart failure and gradually Back[healthfrom.com] Postcholecystectomy syndrome Bile duct / other biliary tree Cholangitis ( PSC, Ascending ) · Cholestasis / Mirizzi's syndrome · Biliary fistula · Haemobilia · Gallstones / Cholelithiasis[wikidoc.org] […] in CHF The congested liver is usually enlarged and firm, often associated with slight enlargement of the spleen Modest elevations of ALT, AST, LDH, r-GT,ALP, T-Bil small decreases[powershow.com]

    Missing: Mutation in the CDK6 Gene

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