Rheumatic Fever
- Pharyngeal Infection with Strep Pyogenes (Group A Strep)
- Rheumatic Heart Disease
- Aschoff Bodies
- Anitschkow's Cells
- Early Death Due to Myocarditis
- Migratory Polyarthritis
- Subcutaneous Nodules
- Erythema Marginatum
- Chorea
- Elevated ESR
Rheumatoid Arthritis Assessment
- Destruction of Connective Tissue and Synovial Membrane
- Inflammation of Joints
- Morning Stiffness
- Nodules
- Joint Deformities
Rheumatoid Arthritis Interventions
- Heat and Cold Applications
- Therapeutic Exercise
- Balance Rest and Activity
- NSAIDs
- DMARDs
- Glucocorticoids
- PT/OT
- Reconstructive Joint Surgery
Anti-desmoglein Antibodies
- Pemphigus Vulgaris
- Flaccid Blisters
- Skin and Oral Mucosa
- Positive Nikolsky's Sign
Anti-glomerular Basement Membrane Antibodies
- Glomerulonephritis
- Goodpasture's Disease
- Linear immunofluorescence
- Hemoptysis
- Hematuria
Anticentromere Antibodies
- Autoimmune Disorders
- CREST Syndrome (Limited Scleroderma)
- Diffuse Scleroderma
Antihistone Antibodies
- Drug-induced Lupus
- SHIPP Acronym
- Sulfonamides
- Hydralazine
- Isoniazid (INH)
- Phenytoin
- Procainamide
Thymic Aplasia (DiGeorge Syndrome)
- DiGeorge Syndrome
- 22q11 Deletion
- Failure to Develop Third and Fourth Pharyngeal Pouches
- Undeveloped Thymus
- T Cell Deficiency
- Recurrent Viral and Fungal Infections
- Undeveloped Parathyroids
- Hypocalcemia
- Tetany
- Aortic Defects
- Congenital Heart Defects
- Absent Thymic Shadow on CXR
IL-12 Receptor Deficiency
- IL-12 Secreted by Macrophages
- Decreased Th1 Response
- Decreased IFN Gamma
- Mycobacterial Infections
- Salmonella
Hyper IgE Syndrome
- Job Syndrome (Autosomal Dominant Hyper IgE Syndrome)
- Autosomal Dominant
- STAT3 Mutation
- Increased IgE
- Abnormal Chemotaxis
- Leonine Facies
- Cold (Non-Inflamed) Staph Aureus Abscesses
- Retained Primary Teeth
- Eczema
- Prophylactic Antibiotics
Hyper IgM Syndrome
- Deficient CD40 Ligand on Helper T-cells
- Defective CD40 Receptor on B-cells
- Inability to Class Switch
- Pyogenic Abscess
- Decreased IgG, IgA, IgE
Selective IgA Deficiency
- Defect in Class Switching
- Decreased IgA
- Often Asymptomatic
- Increase in Atopic & Autoimmune Diseases
- Sinopulmonary Infections
- Increased Risk Giardia Lamblia Infections
- Inflammatory Bowel Disease
- Celiac Disease
- Anaphylaxis From IgA Containing Blood Products
Leukocyte Adhesion Deficiency
- Autosomal Recessive
- Integrin CD18 Protein
- Defect in LFA-1
- Attached to ICAM
- Neutrophilia
- Bacterial Infections
- Non-Pyogenic
- Delayed Separation of Umbilical Cord
Common Variable Immunodeficiency
- Defect in B Cell Maturation
- Decreased Plasma Cells
- Decreased Immunoglobulins
- Sinopulmonary Infections
- Increased Risk of Autoimmune Disease
- Lymphoma
Severe Combined Immunodeficiency (SCID)
- Both B and T Cell Deficiency
- Recurrent Viral, Bacterial, Fungal, Protozoal Infections
- Defective Interleukin (IL) 2 Receptor
- X-Linked
- Adenosine Deaminase Deficiency
- Failure to Synthesize MHC II Antigens
- Treat with Bone Marrow Transplant
Chediak-Higashi Syndrome
- Autosomal Recessive
- Defective Lysosomal Trafficking Regulator Gene (LYST)
- Defect In Microtubular Function
- Decrease In Phagocytosis
- Recurrent Pyogenic Infections
- Staph Aureus And Streptococci
- Partial Albinism
- Peripheral Neuropathy
- Pancytopenia
- Giant Granules In Granulocytes And Platelets
Bruton's Agammaglobulinemia
- X-linked Recessive
- Defective Bruton Tyrosine Kinase
- Blocks B Cell Maturation
- Decreased Immunoglobulins of All Classes
- Bacterial Infections After Six Months
- Maternal IgG Protects Before Six Months
Wiskott Aldrich
- X-linked Recessive
- WASp Protein Mutation
- Antigen Presentation Defect
- Progressive Deletion of B and T Cells
- Thrombocytopenia
- Eczema
- Infections
- Decreased IgM
- Increased IgE, IgA
Ataxia Telangiectasia
- Autosomal Recessive
- ATM Gene
- Defect in DNA repair
- Cerebellar defects
- Spider Angiomas
- Sensitive to Radiation
- Defective Tumor Suppressor Gene
- Increased risk of Cancer, Leukemias, and Lymphomas
- Increased AFP levels
- IgA deficiency
- Repeated sinopulmonary infections
Chronic Mucocutaneous Candidiasis
- T Cell Dysfunction
- Candida Albicans
- Infections of Skin
- Infections of Mucous Membrane
- Susceptible to HPV Infections like Condyloma Acuminatum
Chronic Granulomatous Disease
- Most Commonly X-linked Recessive
- Defective NADPH Oxidase (Enzyme Complex)
- Decreased Hydrogen Peroxide
- Impaired Intracellular Killing in Phagocytes
- Recurrent Purulent Skin and Lung Infections
- Catalase Positive Organisms
- Negative Nitroblue Tetrazolium Test
- DHR (Dihydrorhodamine) Flow Cytometry
- Antimicrobial Prophylaxis
- TMP-SMX
- Itraconazole
- Interferon-Gamma
Complement Disorders
- Early Complement Deficiency
- Pyogenic Infections
- SLE
- Sinus Infections
- Terminal Complement Deficiency
- Autosomal Recessive
- Neisseria Infections
- C5-C9
- MAC (Membrane Attack Complex)
C1 Esterase Inhibitor Deficiency
- Autosomal Dominant
- Disinhibition of Kallikrein
- Increased Bradykinin
- Decreased C4
- Recurrent Angioedema
- Upper Airway Obstruction
- ACE Inhibitors Contraindicated
- Avoid Triggers