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14 Possible Causes for Hepatic Encephalopathy, Intermittent Jaundice, Uric Acid Increased

  • Hepatorenal Syndrome

    Wui-Chiang Lee, Han-Chieh Lin, Ming-Chih Hou, Hsiao-Yi Lin, Fa-Yauh Lee, Sun-Sang Wang, Full-Young Chang and Shou-Dong Lee , Serum Uric Acid Levels in Patients With Cirrhosis[] The pooled rate of hepatic encephalopathy after transjugular intrahepatic portosystemic shunt was 49%.[] Severe circulatory dysfunction (mean arterial pressure usually is 70 mm Hg) and very low systemic vascular resistance. • Severe liver disease, with jaundice, coagulopathy,[]

  • Primary Biliary Cirrhosis

    Twenty four hour urine demonstrated a low renal fractional tubular reabsorption of phosphate, increased fractional excretion of uric acid and generalized aminoaciduria.[] Patients may even present with ascites, hepatic encephalopathy and/or esophageal variceal hemorrhage.[] Reddy AN, Grosberg SJ, Wapnick S: Intermittent cholestatic jaundice and nonmetastatic prostatic carcinoma. Arch Intern Med 1977;137:1616–1618.[]

  • Congenital Liver Cirrhosis

    acid level elevated Maternal mortality, 1%; prematurity and fetal death, 5%-30% Beta blocker, methyldopa, magnesium sulfate; early delivery HELLP syndrome Beyond 22 wk and[] encephalopathy, portal hypertension with ascites and gastrointestinal bleeding, hepatorenal syndrome, HCC development and others.[] He had intermittent high grade fever with dry cough and respiratory distress for 4 days duration.[]

  • Renal Impairment

    […] in uric acid excretion, serum creatinine, or BUN.[] […] spontaneous bacterial peritonitis (except for prophylactic treatment with norfloxacin); the absence of other infections, shock, gastrointestinal bleeding, ileus, grade 3 or 4 hepatic[] Abstract Benign recurrent intrahepatic cholestasis (BRIC) is a rare autosomal recessive condition characterized by intermittent episodes of pruritus and jaundice that may[]

  • Pericholangitis

    acid stones Migratory arthritis Sacroiliitis and ankylosing spondylitis Erythema nodosum and uveitis Complications Toxic megacolon Adenocarcinoma of the colon (1-16%) Increased[] […] resection)肝切除術 hepatic artery 肝動脈 hepatic coma肝性昏睡 hepatic encephalopathy肝性脳症 hepatic failure肝不全 hepatic fibrosis肝線維化 hepatic hemangioma肝血管腫 hepatic lobe肝葉 hepatic regeneration[] Clinically, this condition usually manifests with chronic intermittent obstructive jaundice. Abdominal pain, pruritus, fatiguability and fever are variably present.[]

  • Progressive Retinal Dystrophy due to Retinol Transport Defect

    […] serum uric acid levels. ( 27151312 ) Solak B....Solak Y. 2016 15 Relationship between acne vulgaris and attention-deficit/hyperactivity disorder symptoms in a clinical sample[] Depressivity Encephalopathy Delayed speech and language development Increased circulating cortisol level Chronic active hepatitis Chronic atrophic gastritis Female hypogonadism[] Development and Severity of Acne Vulgaris in a Nigerian Population. ( 27600928 ) Ikaraoha C.I....Amah H.C. 2016 14 Isotretinoin use for acne vulgaris is associated with increased[]

  • Tyrosinemia

    The tubular handling of phosphorus, uric acid, beta 2-microglobulin, and amino acids was disturbed. Low urinary osmolality was also seen.[] He suffered from end-stage liver failure, hypoglycemia and hepatic encephalopathy.[] The acute onset may be dramatic, with hepatomegaly, jaundice, epistaxis, melaena, purpuric lesions, marked oedema, and the distinctive cabbage-like odour.[]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    An acid urine pH favors production of poorly soluble uric acid over the more soluble urate, increasing the risk for precipitation of intratubular uric acid crystals.[] , hepatic encephalopathy and even death.[] To determine whether you have an inherited G6PD deficiency When a child experienced persistent jaundice as a newborn for unknown reasons; when you have had one or more intermittent[]

  • Cross Syndrome

    The elevated serum uric acid (SUA) level is correlated with the metabolic risk of cardiovascular.[] […] failure Retinal dystrophy Hepatic steatosis Diffuse white matter abnormalities Atrophy of the spinal cord Silver-gray hair Encephalopathy Abnormal cerebellum morphology Gliosis[] Type Vd: hepatosplenomegaly and storage signs Intrauterine growth retardation Babies born to mothers with acute fatty liver of pregnancy and HELLP syndrome Intermittent Late-Onset[]

  • Beta-Ureidopropionase Deficiency

    Plasmodium falciparum (malaria parasite) Along with many other disease causing parasites -Juvenile gout -No salvage of purines, therefore causing an increase in uric acid[] […] infancy Hemiconvulsion-hemiplegia-epilepsy syndrome Rasmussen encephalitis Idiopathic macular hole Multiple sclerosis Neuromyelitis optica Spondyloocular syndrome (SOS) Hepatic[] Intellectual disability, seizures, and periodic loss of balance and coordination (intermittent ataxia).[]

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