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370 Possible Causes for Acute Cholecystitis, Autosomal Recessive

  • Erythropoietic Protoporphyria

    […] effect from the mutant FECH allele. 25 The prevalence of autosomal recessive EPP has not been established.[] […] and chronic cholecystitis Chronic liver conditions, such as scarring and fibrosis, due to liver toxicity How is Erythropoietic Protoporphyria Treated?[] EPP is inherited in an autosomal recessive manner.[]

  • Hereditary Spherocytosis

    […] spherocytosis on repeated blood films, Coombs-negative hemolytic jaundice and normal MCHC and MCV measurements, where SDS-PAGE revealed alpha-spectrin deficiency, a rare autosomal-recessive[] Pigmented gallstones (calcium bilirubinate) Elevated reticulocyte count, indirect bilirubin, serum LDH Treatment : Folic acid supplementation Splenectomy Complications : Acute[] This condition can also be inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations.[]

  • Familial Mediterranean Fever

    Primary ciliary dyskinesia (PCD) is a rare disease, predominantly inherited as an autosomal recessive, with ciliary dysfunction leading to impaired mucociliary clearance,[] Laparoscopic intervention in pregnant patients with surgical abdomen such as acute cholecystitis is the optimal method of treatment.[] […] usually autosomal recessive inherited inflammatory disorder caused by mutations in the mefv gene.[]

  • Cystic Fibrosis

    From Wikidata Jump to navigation Jump to search autosomal recessive disease that is characterized by the buildup of thick, sticky mucus that can damage many organs.[] Abstract Cystic fibrosis is an autosomal recessive disease with a prognosis determined by the extent of pulmonary lesions.[] CF mucoviscidosis CYSTIC FIBROSIS CYSTIC FIBROSIS; CF edit Language Label Description Also known as English cystic fibrosis autosomal recessive disease that is characterized[]

  • Acute Hepatic Porphyria

    Patients are most often composite heterozygous and transmission is autosomal recessive.[] […] acid which is autosomal recessive).[] ALA dehydratase deficiency is inherited in an autosomal recessive manner.[]

  • Sickle Cell Disease

    Abstract Sickle cell disease (SCD) is an autosomal recessive disorder that results in hemolytic anemia related to abnormal hemoglobin and erythrocyte levels.[] Cholelithiasis may be asymptomatic or result in acute cholecystitis, requiring surgical intervention. The liver may also become involved.[] Sickle cell disease (SCD) is an autosomal recessive disorder characterized by production of abnormal hemoglobin S and is associated with high morbidity and mortality.[]

  • Cholelithiasis

    Abstract Gaucher disease is an autosomal recessively inherited lysosomal storage disease in which a deficiency of glucocerebrosidase is associated with the accumulation of[] Medication List About Cholelithiasis with Acute Cholecystitis: Cholelithiasis is the presence of gallstones in the gallbladder.[] Abstract Neonatal Bartter syndrome (NBS) is a rare autosomal recessive renal tubular disorder.[]

  • Cooley's Anemia

    recessive trait requiring that both parents pass on a copy of the defective gene located on the chromosome numbered 11.[] Early recognition and stabilization of acute complications—i.e., sepsis, transfusion reactions, drug reactions, or cholecystitis—require close communication between the primary[] Wikipedia: Thalassemia thalassaemia forms of inherited autosomal recessive blood disorders that originated in the Mediterranean region.[]

  • Diabetes Mellitus

    In autosomal dominant inheritance, a child who has a parent with a mutation has a 50% chance of inheriting that mutation. Autosomal recessive.[] Thiamine-responsive megaloblastic anemia (TRMA) syndrome is an autosomal recessive inherited disorder characterised by a triad of megaloblastic anemia, diabetes mellitus,[] Friedreich ataxia (FRDA) is a multisystem autosomal recessive disease with progressive clinical course involving the neuromuscular and endocrine system.[]

  • Obesity

    There are many patients from consanguineous families in whom severe obesity segregates in an autosomal recessive manner and in whom mutations in the known obesity genes have[] The disorder is autosomal recessive and manifested by severe obesity and hyperphagia accompanied by metabolic, neuroendocrine, and immune dysfunction. [53] It is exquisitely[]

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