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2,779 Possible Causes for No Hepatomegaly

  • Infantile Hepatic Hemangioendothelioma

    We report a case of hepatic hemangioendothelioma in an 8- month-old female infant who presented with hepatomegaly and respiratory distress, which was successfully treated[] We report a case of a 2 1/2-year-old girl presenting with abdominal pain, fever, vomiting, and hepatomegaly.[] The authors describe a 10-week-old girl with infantile hepatic hemangioendothelioma who initially presented with difficulty feeding, hepatomegaly, and multiple hemangiomas[]

  • Hepatosplenomegaly

    Hepatomegaly in the absence of signs of CLD is unlikely to be due to cirrhosis. Consider a malignancy instead.[] In the second case, the hepatomegaly was moderate, and with conservative treatment in the neonatal period the outcome was good.[] Hepatomegaly/parasitology* Humans Kenya Leukocytes, Mononuclear/immunology Malaria, Falciparum/complications* Malaria, Falciparum/immunology Malaria, Falciparum/pathology[]

  • Congenital Hepatic Fibrosis

    The age at presentation ranged from 1.8-14 years (mean: 7.5 years); clinical manifestations at diagnosis were splenomegaly (12), hepatomegaly (11), failure to thrive (10),[] Hepatomegaly was present in all patients and splenomegaly in all but one.[] Two children with congenital hepatic fibrosis presented atypically: one with prolonged fever and hepatomegaly associated with a giant intrahepatic biliary cyst and a second[]

  • Mauriac's Syndrome

    Mauriac's syndrome should be considered in subjects with brittle type 1 diabetes and hepatomegaly.[] Growth rate improved significantly and hepatomegaly regressed. Puberty progressed rapidly in two older patients with poor final height.[] Increase of hepatic enzymes and hepatomegaly at physical examination (4 confirmed by ultrasonography) were present in all the patients.[]

  • Glycogen Storage Disease

    They were ultimately found to have hepatomegaly, fasting hypoglycemia, mild elevation of transaminases and ketosis.[] The child presented with progressive abdominal swelling due to marked hepatomegaly.[] Most patients with the disease are thought to outgrow the childhood manifestations, which include hepatomegaly, poor growth, and ketosis with or without hypoglycemia.[]

  • Glycogen Storage Disease Type 6

    Hepatomegaly and hypoglycemia are common consequences, although the symptoms are usually mild.[] Hepatomegaly usually improves with age and disappears entirely at puberty.[] Findings from imaging studies may reveal hepatomegaly. Liver biopsy may be required to diagnose the cause of hepatomegaly.[]

  • Glycogen Storage Disease due to GLUT2 Deficiency

    Most patients have the typical combination of clinical symptoms: hepatomegaly secondary to glycogen accumulation, glucose and galactose intolerance, fasting hypoglycemia,[] Here we report a follow up of this original patient over more than 50 years and show that the typical clinical and laboratory findings of FBS (hepatomegaly secondary to glycogen[]

  • Cholesterol Ester Storage Disease

    Increased levels of cholesterol and hepatomegaly were the first findings.[] The third affected sibling, followed to 13 years of age, has hepatomegaly, hyperlipidemia, short stature, adrenal calcification, and acid lipase deficiency.[] An adult patient is described with hepatomegaly and sea-blue histiocytes in the bone marrow.[]

  • Glycogen Storage Disease Type 1

    The syndrome results in hepatomegaly secondary to glycogen accumulation, glucose and galactose intolerance, fasting hypoglycaemia, a characteristic proximal tubular nephropathy[] Abstract A male child presented at 5 months of age with vomiting, diarrhoea, hypoglycaemia and hepatomegaly.[] The molecular pathways involved in liver pathologies, including steatosis, hepatomegaly (glycogenic hepatopathy) and the development of liver tumours are also compared.[]

  • Glycogen Storage Disease Type 3

    Hepatomegaly and growth retardation are other common features.[] GSD III is characterized by fasting hypoglycemia, hepatomegaly, growth retardation, progressive myopathy, and cardiomyopathy due to storage of abnormally structured glycogen[] Clinically, patients with GSD III present in infancy or early childhood with hepatomegaly, hypoglycemia, and growth retardation.[]

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