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1,365 Possible Causes for Liver Enzymes Abnormal

  • Citrullinemia Type 2

    Urea cycle enzyme disorders are liver based metabolic disorders and liver transplantation is, therefore, an ideal treatment.[jnnp.bmj.com] The optimal goal of treatment in metabolic encephalopathy is to correct the underlying abnormal metabolism in the patient before irreversible brain damage occurs.[jnnp.bmj.com]

  • Cerebral Angiitis

    Multicentric Castleman's disease (MCD) is characterized by a systemic lymphoproliferative disorder affecting systemic lymph nodes. Cerebrovascular involvements have rarely been reported, and to our knowledge, cerebral angiitis causing subarachnoid hemorrhage (SAH) in patients with Multicentric Castleman's disease[…][ncbi.nlm.nih.gov]

  • Malaria

    Malaria is a major cause of death worldwide and is brought about by the protozoan parasite Plasmodium acquired from a bite of a female Anopheles mosquito carrier. Malaria are still endemic in warm climates and in most third world countries around the globe. It is essentially non-existent in highly developed and first[…][symptoma.com]

  • Biliary Atresia

    Diagnosis is often made following investigation of prolonged jaundice that is resistant to phototherapy and/or exchange transfusions and abnormalities in liver enzymes tests[checkorphan.org] Diagnosis is often made following investigation of prolonged jaundice that is resistant to phototherapy and/or exchange transfusions, with abnormalities in liver enzyme tests[en.wikipedia.org] Diagnosis - Biliary atresia Diagnosis is made by assessing an individual's symptoms, physical exam, and medical history, in conjunction with blood tests, a liver biopsy and[checkorphan.org]

  • Congenital Generalized Lipodystrophy Type 4

    Congenital generalized lipodystrophy type 4 (CGL4) is a rare metabolic disorder inherited in an autosomal recessive pattern. It has been related to mutations of the PTRF or CAVIN1 gene. Affected individuals are greatly lacking body fat, and this condition may be apparent at birth or develop during childhood.[…][symptoma.com]

  • Carnitine Transporter Deficiency

    Systemic primary carnitine deficiency ( SPCD ), [1] is an inborn error of fatty acid transport caused by a defect in the transporter responsible for moving carnitine across the plasma membrane. Carnitine is an important amino acid for fatty acid metabolism. [4] When carnitine cannot be transported into tissues,[…][en.wikipedia.org]

  • Mitochondrial Trifunctional Protein Deficiency

    Mitochondrial trifunctional protein deficiency Mitochondrial trifunctional protein deficiency has an autosomal recessive pattern of inheritance Types Mutations in the HADHA and HADHB gene - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 12 November 2016. a b "Home - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 12 November[…][en.wikipedia.org]

  • Aggressive Systemic Mastocytosis

    Summary Epidemiology It represents less than 10% of cases of SM and the global prevalence is estimated in the order of between 1/400,000 and 1/250,000. Clinical description ASM doesn't usually develop in children. Cutaneous involvement is normally absent. Patients present with severe symptoms related to mast cell[…][orpha.net]

  • Severe Aplastic Anemia

    Optimal modalities for immunosuppressive therapy (IST) for severe aplastic anemia (SAA) have to be determined, and especially cyclosporine (CyA) dosing to promote regulatory T cells (Treg) which are lacking and which account for physiopathological mechanisms. We are reporting on three cases of pediatric patients[…][ncbi.nlm.nih.gov]

  • Vaginal Candidiasis

    Therapy with the oral azoles has been associated rarely with abnormal elevations of liver enzymes.[cdc.gov]

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