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3,807 Possible Causes for CD27+ B Cells Decreased, Desbuquois Dysplasia, Hepatomegaly

  • Immunodeficiency Type 23

    […] resembling Desbuquois dysplasia.[] Additional symptoms can include vomiting, diarrhea, abdominal pain, and an enlarged liver (hepatomegaly).[] Gastrointestinal manifestations (GIT) of the congenital glycosylation disorders have included deranged liver function, hepatomegaly, liver fibrosis, steatosis and protein-losing[]

  • Chronic Alcoholism

    The distribution of PB B-cell subsets (immature/regulatory, naïve, CD27(-) and CD27( ) memory B lymphocytes, and circulating plasmablasts of distinct immunoglobulin-Ig-isotypes[] Hepatomegaly (in chronic alcoholic liver disease the liver is shrunken). Ascites; gonadal atrophy. Atrial fibrillation and cardiomyopathy.[] Characteristic ultrasonographic findings include a hyperechoic liver with or without hepatomegaly.[]

    Missing: Desbuquois Dysplasia
  • Chronic Lymphocytic Leukemia

    […] of CD25 /CD127 cells.[] 0 lymphocytosis in the blood and marrow only (survival 120 months) Stage I lymphocytosis and adenopathy (survival 95 months) Stage II lymphocytosis, splenomegaly and/or hepatomegaly[] […] 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[]

    Missing: Desbuquois Dysplasia
  • Systemic Lupus Erythematosus

    There is decreased suppression of memory B cells with increased CD27 /IgD- which is related to increased disease activity and renal lupus [ 6, 7, 8 ].[] Other signs are: Pancreatitis, Lupus Enteropathy, Hepatitis and Hepatomegaly 5. Systemic Fever, Malaise/Fatigue, Lymphadenopathy, Weight loss 6.[] Polyclonal B-cell activation occurs in SLE and a shift towards immature B cells.[]

    Missing: Desbuquois Dysplasia
  • Severe Combined Immunodeficiency

    […] resembling Desbuquois dysplasia.[] 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: CD27+ B Cells Decreased
  • Glycogen Storage Disease Type 0

    dysplasia 2; Desbuquois 異形成2) XYLT1 DDD2 (Dowling-Degos disease 2; ダウリング-デゴス病2) POFUT1 EDSP1(Ehlers-Danlos 症候群, プロゲロイド型, 1; エーラスダンロス症候群I型) B4GALT7 EDSP2 (Ehlers-Danlos syndrome[] The diagnosis of GSD0 should be considered in a child with ketotic fasting hypoglycemia with postprandial hyperglycemia but without hepatomegaly.[] Patients present with morning fatigue and fasting hypoglycemia (without hepatomegaly) associated with hyperketonemia but without hyperalaninemia or hyperlactacidemia.[]

    Missing: CD27+ B Cells Decreased
  • Hepatitis B

    Only in T-Group, Chinese medicine symptom complex score and the frequency of total B cells were significantly decreased, and the frequencies of Bm1, CD24 CD27-switched B cells[]

    Missing: Desbuquois Dysplasia
  • Hypogammaglobulinemia

    CD19 CD27 memory B cells and IgM-IgD-CD27 switched B cells are decreased in many of the B-cell immunodeficiencies, such as CVID, HIGM syndrome, and selective antibody deficiency[] The frequency of transitional B cells decreases over time, while the frequency of naive B cells remains stable ( Figure 2B ).[] Memory and switched B cells.[]

    Missing: Desbuquois Dysplasia
  • Mycosis Fungoides

    RESULTS: The frequency of CD19 CD24 hi CD27 B cells, CD19 CD24 hi CD38 hi B cells, and IL-10-producing B cells was decreased in peripheral blood of advanced MF patients.[] Liver involvement may be suggested by clinical hepatomegaly, abnormal liver function tests, or radiologic tests (CT, fludeoxyglucose-positron emission tomography, and liver[] The correlation between frequency or number of B-cell subsets and disease severity markers was also analysed.[]

    Missing: Desbuquois Dysplasia
  • Geleophysic Dysplasia

    dysplasia XYLT1 Desbuquois dysplasia type 2[] Acromicric dysplasia (AD) and geleophysic dysplasia (GD) are rare skeletal dysplasias characterized by short stature, acromelia, joint contracture, hepatomegaly, hoarseness[] […] geleophysic dwarfism: small stature, a peculiar but pleasant and good-natured facial appearance, a dysostosis-multiplex-like bone dysplasia affecting predominantly hands and feet, hepatomegaly[]

    Missing: CD27+ B Cells Decreased

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