Matching
Match the deficiency disease with its specific abnormality.
Premises:
DiGeorge’s syndrome
Severe combined immunodeficiency
Bare lymphocyte syndrome (MHC class I)
Chronic granulomatous disease
X-linked agammaglobulinemia
Leukocyte adhesion deficiency
Hereditary angioneurotic edema
X-linked hyper IgM syndrome
Responses:
Defective CD40 ligand
Defective Btk tyrosine kinase
Defective NADPH oxidase
Defective C1 inhibitor
Thymic aplasia
Defective CD18
Defective RAG1 or RAG2
Defective transporter associated with antigen processing (TAP)
Correct Answer:
Premises:
Responses:
DiGeorge’s syndrome
Severe combined immunodeficiency
Bare lymphocyte syndrome (MHC class I)
Chronic granulomatous disease
X-linked agammaglobulinemia
Leukocyte adhesion deficiency
Hereditary angioneurotic edema
X-linked hyper IgM syndrome
Premises:
DiGeorge’s syndrome
Severe combined immunodeficiency
Bare lymphocyte syndrome (MHC class I)
Chronic granulomatous disease
X-linked agammaglobulinemia
Leukocyte adhesion deficiency
Hereditary angioneurotic edema
X-linked hyper IgM syndrome
Responses:
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