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867 Possible Causes for Hereditary Spherocytosis, Liver Disease

  • Nail Abnormality

    This can be the result of low oxygen in the blood and is associated with: cardiovascular diseases inflammatory bowel disease liver diseases pulmonary diseases AIDS Nonuniform[] It is also associated with inflammatory bowel disease, cardiovascular disease, liver disease and AIDS. Terry's Nails This was named for Dr.[] disease But don't self-diagnose – see a GP if you're worried.[]

  • Congenital Chloride Diarrhea

    Pediatric Gastrointestinal and Liver Disease, by Drs. Robert Wyllie and Jeffrey S. Hyams provides the comprehensive reference you need to treat GI diseases in children.[] Duygu Akçay, Bülent Devrim Akçay DOI : 10.24953/turkjped.2018.03.004 Hereditary spherocytosis: Retrospective evaluation of 65 children.[] Make optimal use of the newest techniques, technologies, and treatments with Sleisenger and Fordtran's Gastrointestinal and Liver Disease - the indispensable information source[]

  • Bone Marrow Aspiration

    The sensitivity of bone marrow aspirate for the diagnosis of NPC disease in patients presenting with infantile liver disease was lower than previously reported.[] spherocytosis Increased plasma cells may indicate: Cancer Liver disease or cirrhosis Connective tissue disorder Allergic reaction Infection Macroglobulinemia Ulcerative colitis[] To review our experience of bone marrow aspiration in children with NPC presenting with infantile liver disease.[]

  • Red Cell Aplasia

    Apply the latest know-how on heparin-induced thrombocytopenia, stroke, acute coronary syndromes, hematologic manifestations of liver disease, hematologic manifestations of[] ., sickle cell anemia, hereditary spherocytosis, and pyruvate kinase deficiency Etiology temporary cessation of RBC production with a viral infection of erythroid progenitors[] Lefrere JJ, Conronce A-M, Girot R, et al: Six cases of hereditary spherocytosis revealed by human parvovirus infection. Br J Haematol 62:653, 1986. 10.[]

  • Deferoxamine

    Features of iron metabolism are presented, and this infant's illness is contrasted with other liver diseases of infancy associated with hepatic iron overload.[] A 76-year-old man with paroxysmal nocturnal hemoglobinuria and hereditary spherocytosis was started on deferoxamine for iron overload secondary to previous blood transfusions[] The patients lacked the usual predisposing factors to mucormycosis, ie, diabetes and acidosis, but both had liver disease.[]

  • Hypersplenism

    Patients with liver disease also have abnormalities in coagulation.[] Haemolysis: hereditary spherocytosis, sickle cell anaemia, thalassaemia.[] spherocytosis) Advertisement[]

  • Viral Hepatitis

    A total of 140 patients (67 thalassemic patients, 70 hemophilic patients, two patients with hereditary spherocytosis and one patient with von Willebrand disease) were prospectively[] We present two consensus definitions of advanced and late stage liver disease being used as epidemiological tools.[] disease or exacerbates, even at high doses, serious pre-existing liver disease.[]

  • Portal Vein Thrombosis

    Patients with chronic liver disease and PVT with a suspicion of HCC referred for EUS-FNA were included.[] Patients with big spleens (mostly patients with myelofibrosis or lymphoma) and patients with hemolysis, in particular hereditary hemolytic anemias (hereditary spherocytosis[] “In patients with cirrhosis, the development of PVT is associated with the severity of liver disease at baseline, but does not follow a recent progression of liver disease[]

  • Glossitis

    Oral disease and oral-cutaneous manifestations of gastrointestinal and liver disease. In: Feldman M, Friedman LS, Brandt LJ, eds.[] Sleisenger and Fordtran's Gastrointestinal and Liver Disease . 10th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 24.[]

  • Viremia

    Not linked to disease severity Viral factors appear to be predictive of Hepatitis C virus-recurrent disease but not disease severity in patients who have undergone liver transplantation[] A 31-year-old man, who had undergone splenectomy 18 months previously because of hereditary spherocytosis, suddenly became ill, with fever, vomiting, epigastric pain and shock[] , National Institutes of Health, DHHS , Bethesda, Maryland , USA 2 Liver Diseases Branch , National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes[]

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