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3,699 Possible Causes for Hepatomegaly, Immunoglobulin M Decreased, Postural Defect

  • Amyloidosis

    Hepatic involvement is common, but the clinical manifestations are usually mild with hepatomegaly and an elevated alkaline phosphatase level.[] Flies carrying mutant variants, but not wild-type TTR, exhibit changes in wing posture, locomotor defects, and shortened life span.[] […] that presents to a cancer care provider with nephrotic range proteinuria, heart failure with preserved ejection fraction, non-diabetic peripheral neuropathy, unexplained hepatomegaly[]

  • Hepatocellular Carcinoma

    Otherwise, presentation may include: constitutional symptoms jaundice portal hypertension from the invasion of the portal vein hepatomegaly/mass hemorrhage from tumor The[] Vital signs were within normal limits, and there was tender hepatomegaly.[] Physical examination disclosed midepigastric tenderness and tender hepatomegaly.[]

    Missing: Postural Defect
  • Chronic Lymphocytic Leukemia

    […] of the left zygomatic region; anterior nasal bleeding; pustulous non-itching lesions at the cervical region and posterior thorax; enlarged bilateral axillary lymph nodes; hepatomegaly[] Patients may sometimes present with hepatomegaly , splenomegaly or both and/or a hemolytic anemia .[] Patients may sometimes present with hepatomegaly, splenomegaly or both and/or hemolytic anemia.[]

    Missing: Postural Defect
  • Chronic Myeloid Leukemia

    Hepatomegaly also occurs, although less commonly than splenomegaly. Hepatomegaly is usually part of the extramedullary hematopoiesis occurring in the spleen.[] Low-grade fever and excessive sweating Elevated white blood cell (WBC) count Splenomegaly Decreased appetite and food intake Left upper quadrant abdominal pain from splenomegaly Hepatomegaly[] Poor-prognosis characteristics include the following clinical and laboratory factors: Older age Symptomatic presentation Poor performance status African-American descent Hepatomegaly[]

    Missing: Postural Defect
  • Chronic Phase of Chronic Myeloid Leukemia

    Hepatomegaly. Enlarged lymph nodes are also a possibility. Anaemia can produce a hyperdynamic circulation. Easy bruising. Fever. Gout due to rapid cell turnover.[] Poor-prognosis characteristics include the following clinical and laboratory factors: Older age Symptomatic presentation Poor performance status African-American descent Hepatomegaly[] Symptoms may include unexplained fever, bone pain, splenomegaly, and hepatomegaly.[]

    Missing: Postural Defect
  • Adenosine Deaminase Deficiency

    A year later she developed hepatomegaly, cholecystitis, and cholelithiasis. Liver biopsy specimens showed granulomas of undetermined cause.[]

    Missing: Postural Defect
  • Severe Combined Immunodeficiency

    Systemic examination was remarkable with spleno-hepatomegaly but other systems were essentially normal.[] There may be hepatomegaly, with or without splenomegaly, particularly when disseminated Bacille Calmette–Guerin (BCG) infection is present.[]

    Missing: Postural Defect
  • Hypogammaglobulinemia

    Serum immunoglobulin determination at Walter Reed General Hospital revealed an immunoglobulin G level of 150 mg per 100 ml and absence of immunoglobulins A and M.[] Norlin AC, Sairafi D, Mattsson J, Ljungman P, Ringden O, Remberger M. Allogeneic stem cell transplantation: low immunoglobulin levels associated with decreased survival.[] Tomblyn M, Chiller T, Einsele H, Gress R, Sepkowitz K, Storek J, et al.[]

    Missing: Postural Defect
  • Kwashiorkor

    The child presented at 10 months of age with decreased weight for height, rash, hepatomegaly, edema, hypoproteinemia, hypoalbuminemia, anemia, hypoglycemia, and evidence of[] Complications Some complications of kwashiorkor include: Hepatomegaly (from the fatty liver) Cardiovascular system collapse/hypovolemic shock Urinary tract infections Abnormalities[] In severe cases, hepatomegaly can occur due to decreased production of lipoprotein.[]

    Missing: Postural Defect
  • Ataxia Telangiectasia

    (NGS) was performed on an Iranian 5-year-old boy presented with truncal and limb ataxia, telangiectasia of the eye, Hodgkin lymphoma, hyper pigmentation, total alopecia, hepatomegaly[] Defects in speech Spider-like veins visible along the skin and eyes Recurrent lung, sinus, and ear infection Slow physical and sexual maturation How is Ataxia Telangiectasia[] 象徴不能/失象徴 asymmetrical septal hypertrophy 非対称性中隔肥大/非対称性心室中隔肥大 ASH asymptomatic bacteriuria 無症候性細菌尿 asymptomatic diabetes 無症候性糖尿病 asymptomatic hematuria 無症候性血尿 asymptomatic hepatomegaly[]

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