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11 Possible Causes for Conduction Disorder of the Heart, Liver Enzymes Abnormal, Steatorrhea

  • Hemochromatosis

    The disease is usually diagnosed as a result of family screening or after a blood test indicates a high level of iron or abnormal liver enzymes.[hopkinsmedicine.org] Mild liver enzyme abnormalities: eliminating hemochromatosis as a cause. Clin Chem 1997 ; 43 : 1535 -1538. Barton JC, Grindon AF, Barton NH, Bertoli LF.[clinchem.aaccjnls.org] Furthermore, liver biopsy is also recommended for compound heterozygotes with elevated TS and abnormal liver enzyme levels or clinical evidence of liver disease.[clevelandclinicmeded.com]

  • Amyloidosis

    Generally, the amyloid-infiltrated liver feels very hard, and elevated liver enzymes (particularly alkaline phosphatase) and other liver function abnormalities may be detected[rarediseases.org] The symptoms include diarrhea, steatorrhea, or constipation. Pseudo-obstruction carries a particularly grave prognosis, often not responding to pro-motility agents.[ncbi.nlm.nih.gov] Microscopic examination of a stool specimen stained with Sudan III showed steatorrhea with no evidence of parasites.[scielo.isciii.es]

  • Congenital Heart Block

    There may also be abnormalities of liver enzyme levels and jaundice.[ncbi.nlm.nih.gov] […] block NOS Third degree block congenital Q24.6 congenital Q24.6 heart I45.9 ICD-10-CM Diagnosis Code I45.9 Conduction disorder, unspecified 2016 2017 2018 2019 Billable/Specific[icd10data.com] Mild gastrointestinal abnormalities, mild steatorrhea and excess protein loss are common in infants with CHD. 11 Up to 30 percent of infants with CHD have features of various[aafp.org]

  • Liver Cirrhosis

    […] in the liver); Diseases caused by abnormal liver function, such as hemochromatosis (a condition in which excessive iron is absorbed and deposited into the liver and other[my.clevelandclinic.org] PSC is a progressive cholestatic disorder presenting with pruritus, steatorrhea, fat-soluble vitamin deficiencies, and metabolic bone disease.[en.wikipedia.org] Conduct conduct disorders. Congenital congenital anomalies. COPD chronic obstructive pulmonary disease. Drugs drug use disorders.[ncbi.nlm.nih.gov]

  • Combined Pancreatic Lipase - Colipase Deficiency

    A liver biopsy reveals glycogen with an abnormal, amylopectin- like structure with long outer chains. Which of the following enzymes would most likely be deficient?[passeidireto.com] […] hearing loss-heart defect syndrome Dysmorphism-multiple structural anomalies syndrome Dysmorphism-pectus carinatum-joint laxity syndrome Dysmorphism-short stature-deafness-disorder[orpha.net] Different Groups of Steatorrhea Individuals suffering from steatorrhea may be thinking of the three broad etiologic groups.[steatorrhea.org]

  • Ataxia

    Peroxisomal disorders include: Zellweger syndrome (abnormal facial features, enlarged liver, and nerve damage in infants) Adrenoleukodystrophy (symptoms of nerve damage can[webmd.com] In addition, studies of diabetes and heart disease are being conducted in order to determine their relationship with this neurological disorder.[brainfoundation.org.au] Developmental history Steatorrhea? Has there been increased number of infections of the upper respiratory tract?[pedclerk.bsd.uchicago.edu]

  • Alagille Syndrome

    […] or cardiac disease to only subclinical manifestations, such as mildly abnormal liver enzymes, a heart murmur, butterfly vertebrae, posterior embryotoxon, or characteristic[dovepress.com] Abstract Alagille syndrome (AGS) is often associated with symptoms of maldigestion, such as steatorrhea, hypotrophy and growth retardation.[ncbi.nlm.nih.gov] […] characterized by colobomas of the eye, congenital heart defects, migratory ichthyosiform rash of the skin, mental retardation and ear defects (overfolding helices and conductive[doi.org]

  • Friedreich Ataxia

    Peroxisomal disorders include: Zellweger syndrome (abnormal facial features, enlarged liver, and nerve damage in infants) Adrenoleukodystrophy (symptoms of nerve damage can[webmd.com] In addition, studies of diabetes and heart disease are being conducted in order to determine their relationship with this neurological disorder.[brainfoundation.org.au] One subject with a low body mass index experienced steatorrhea taking a high dose and discontinued the study.[ncbi.nlm.nih.gov]

  • Myopathic Carnitine Deficiency

    […] deficiency: Intermittent episodes of hypoglycemia Abnormal liver function tests Liver and heart enlargement Lactic academia Hyperuricemia Above occur in both entities: Glycogen[neurodiffdx.com] […] and muscle have the lowest threshold Clinical Features of Mitochondrial Disorders Systemic Signs and Symptoms Short stature Diabetes mellitus Pigmentary retinopathy Cardiac[neurodiffdx.com] […] ichthyosis Age of onset: second decade in most patients Ichthyosis: Lamellar ichthyosis Accentuated over the flexor creases Mild erythema in affected area Ectropion (eyelid) Steatorrhea[neurodiffdx.com]

  • Mitochondrial DNA Deletion Syndrome with Progressive Myopathy

    Liver biopsy may show steatosis, abnormal mitochondria, and nonspecific abnormalities. Enzyme analysis of the ETC.[neuropathology-web.org] Cognitive impairment Hepatic steatosis EMG abnormality Chest pain Hypothyroidism Hypertonia Hypolipidemia Vitamin D deficiency Vertical supranuclear gaze palsy Fat malabsorption Steatorrhea[mendelian.co] (cardiomyopathy), especially conduction disorders (e.g., heart block).[rarediseases.org]

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