Disease Information for Immundeficiency, combined B And T cell

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Clinical Manifestations
Signs & Symptoms
Carious teeth/child
Carious teeth/sign
Teeth malformed/dysplastic
Typical Clinical Presentation
Viremia Sepsis with low WBC
Clinical Presentation & Variations
Presentation/Infective Endocarditis Unusual agent Male
Presentation/Resistant Tinea Pedis Corporus
Presentation/Resistant verruca Warts Poor control
Presentation/Lymphopenia Candidal diarrhea
Presentation/Recurrent pneumonia Child
Disease Progression
Course/Chronic disorder
Course/Chronic only
Course/Prognosis bad/usually
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Family History
Family history/Immune defects
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Laboratory Tests
Microbiology & Serology Findings
Common vaccination antibodies absent/low
Abnormal Lab Findings (Non Measured)
Absent/Low B-cells on Flow Cytometry
Chronic lymphopenia
Lymphocyte phenotype/panel abnormal (Lab)
Abnormal Lab Findings - Decreased
Circulating Total T-Cell Count
IGM/Immunoglobulin M (Lab)
Lymphocytes (Lab)
Abnormal Lab Findings - Increased
Gamma globulin (Lab)
Lymphocytes (Lab)
Diagnostic Test Results
Other Tests & Procedures
Skin test anergy
Skin test/DNCB (dinitrochlorobenzene) abnormal
X-RAY
Xray/Chest abnormal
Xray/Chest/Lung fields/Abnormal
Associated Diseases & Rule outs
Associated Disease & Complications
Agammaglobulinemia, acquired
Anergic status
Bronchiectasis
Candida albicans infection
Cellular immunity defect/deficiency
Dental caries
Dental deformities/anomalies
EBV/B-cell Lymphoproliferative syndrome
Fungal skin infections
Giardia infection/intestinal
Hypogammaglobulinemia
Hypogammaglobulinemia, acquired
Intestinal/gut lymphoma
Lymphocytopenia
Lymphocytosis
Neonatal Erythroderma
Nodular lymphatoid hyperplasia/gut
Opportunistic infections triggers/causes
Pneumococcus infection
Pneumocystis Jiroveci/Carinii Pneumonia (PCP)
Pneumonia
Pneumonia, bacterial
Pneumonia, pneumococcal
Pneumonia, recurrent
Pneumonia, unresolved/Chronic
Pneumonia/Bronchopneumonia
Systemic mycosis/disseminated
Teeth enamel hypoplastic
Disease Mechanism & Classification
Class
CLASS/Immune System Disorder (ex)
CLASS/Spleen/thymus/RES/immune system (category)
Pathophysiology
Pathophysiology/Fungal infection prone
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Infection resistant to usual treatments
Pathophysiology/Combined T-cell/B-cell immune deficiency
Pathophysiology/Decreased T Cells
Pathophysiology/Immune physiology/defective
Pathophysiology/Immune/cellular system disorder (ex)
Pathophysiology/Suppressor T-cell activation
Process
PROCESS/Congenital/developmental (category)
PROCESS/Hereditofamilial (category)
PROCESS/Immune system disorder (ex)
Treatment
Drug Therapy - Indication
RX/Gamma globulin/prophylaxis/low dose
SX/Stem cell transplant/allogenic
SX/Stem-cell transplant
Definition

A group of disorders characterized by congenital and usually hereditary deficiency of both B-cell and T-cell systems, lymphoid aplasia, and thymic dysplasia. [merck manual 17th ed]; subsets include X-linked severe combined immunodeficiency or scids, ADA or adenosine deaminase deficiency, and Nezelof syndrome which is "combined immunodficiency with Igs [non-functioning Igs]"

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External Links Related to Immundeficiency, combined B And T cell
Google
Wikipedia
Merck
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PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)
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