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2,507 Possible Causes for Albumin Decreased, Dyspepsia, Mutation in the CDK6 Gene

  • Gastric Adenocarcinoma

    Abstract An elderly Thai woman had presented with dyspepsia and reflux symptoms since 6 years.[] In Pt2, the SETBP1 gene (p.S944N) was mutated, as it is in myeloid malignancies ( 20 ), together with amplification of AKAP9 and CDK6 (cyclin-dependent kinase 6).[] Early stage gastric adenocarcinoma patients have nonspecific symptoms, that usually do not trigger a consultation until the disease has advanced, such as dyspepsia, anorexia[]

  • Liver Cirrhosis

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

    Missing: Mutation in the CDK6 Gene
  • Preeclampsia

    It may also be related to decreased plasma colloid oncotic pressure from proteinuria, use of crystalloids to replace blood loss, and decreased hepatic synthesis of albumin[]

    Missing: Mutation in the CDK6 Gene
  • Celiac Disease

    CD prevalence in adults with functional dyspepsia or irritable bowel syndrome can rise to over 10% of cases, as reported in some studies.[] albumin level Malnutrition Elevated calcium level, decreased phosphate level Vitamin D deficiency, secondary hyperparathyroidism Thrombocytosis, leukocytosis General inflammatory[] […] in albumin levels, and intestinal obstruction .[]

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

    SE Shim, Milan Bassan, Jamshid S Kalantar, Martin D Weltman, Michael Jones, Nicholas Powell and Nicholas J Talley, Duodenal eosinophilia and early satiety in functional dyspepsia[] 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[] […] retention, fat redistribution, hypertension, hyperglycemia, psycho-neurological disturbances, cataracts, growth failure in children, osteonecrosis[ 115 ] Mesalazine Nausea, dyspepsia[]

    Missing: Mutation in the CDK6 Gene
  • Malabsorption Syndrome

    […] most common clinical manifestations of CD include abdominal cramping pain with moderate to severe abdominal distension, frequently associated with relapsing or permanent dyspepsia[] Prothrombin time- Vitamin K level decreased 3. Serum albumin- Decreased (protein loss) 4.[] Albumin is a general indicator of nutritional state. Low albumin can result from poor intake, decreased synthesis in cirrhosis, or protein wasting.[]

    Missing: Mutation in the CDK6 Gene
  • Pancreatic Insufficiency

    […] control; Single small stool sample Sensitivity low for clinical practice (chymotrypsin is variably inactivated during intestinal transit); not for mild EPI; watery stools decrease[] […] resonance cholangiopancreatograpgy Morphological and semi-quantitative functional changes Requires further validation Nutritional status (magnesium 2.05 mg/dL, prealbumin, albumin[]

    Missing: Mutation in the CDK6 Gene
  • Hypertrophic Gastritis

    Characteristically, patients with Ménétrièr's disease are older than 60 years of age and have epigastric pain, weight loss, nausea, diarrhea, and dyspepsia, with or without[] […] increase in the serum albumin concentration and a decrease in the loss of protein in the stool.[] ) Excess mucus secretion in the stomach Decreased acid secretion by the stomach The low level of acid secretion results in a failure to digest proteins and absorb nutrients[]

    Missing: Mutation in the CDK6 Gene
  • Liver Disease

    Laboratory findings may include, but are not limited to, increased liver enzymes, increased serum total bilirubin, increased ammonia levels, decreased serum albumin, and abnormal[] […] coagulation studies, such as increased International Normalized Ratio (INR) or decreased platelet counts.[] Abnormally low serum albumin or elevated INR levels indicate loss of synthetic liver function, with increased likelihood of cirrhosis and associated complications.[]

    Missing: Mutation in the CDK6 Gene
  • Cystic Fibrosis

    Cystic fibrosis (mucoviscidosis) is the most common type of genetic metabolic disease. It leads to the build-up of viscous, high-protein secretion in the body’s glands. This primarily affects the lungs, digestive tract and genitals. There is no causal treatment available for cystic fibrosis at present, but the life[…][]

    Missing: Mutation in the CDK6 Gene

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