IMMUNODEFICIENCIES / IMMUNOLOGIC DISORDERS
Authored by Daverich Hoyle 侯英敏
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42 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • Ungraded
B-CELL: Is a rare genetic disorder that affects the body's ability to fight infection. Absence of BTK gene (Bruton's tyrosine kinase)
Bruton's X-Linked Agammaglobulinemia
Common Variable Immunodeficiency (CVI)
Transient Hypogammaglobulinemia
X-linked Hyper IgM Syndrome
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
B-CELL: Failure of mature B cells to become plasma cells. Unknown mechanism (idiopathic). No antibody production. Congenital presentation; IgA and IgG def. (+) B-cell.
Bruton's X-Linked Agammaglobulinemia
Common Variable Immunodeficiency (CVI)
Transient Hypogammaglobulinemia
X-linked Hyper IgM Syndrome
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
B-CELL: Failure of B cells to produce antibodies due to delayed maturation of thymus. Also referred to as Pediatric Hypogammaglobinemia
Bruton's X-Linked Agammaglobulinemia
Common Variable Immunodeficiency (CVI)
Transient Hypogammaglobulinemia
X-linked Hyper IgM Syndrome
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
B-CELL: Increased levels of IgM. Absence of CD40 ligand on T helper cell
Bruton's X-Linked Agammaglobulinemia
Common Variable Immunodeficiency (CVI)
Transient Hypogammaglobulinemia
X-linked Hyper IgM Syndrome
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
B-CELL: Impaired of IL-2 production. Hyperactive Th2. Prone to allergic reactions.
Hyper IgE
IgA Deficiency
Isolated IgG Subclass Deficiency
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
B-CELL: Most common primary immunodeficiency. Failure of B cells to become IgA-producing plasma cells, Recurrent gastrointestinal and respiratory infection.
Hyper IgE
IgA Deficiency
Isolated IgG Subclass Deficiency
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
B-CELL: Person lacking a specific IgG subclass -> vulnerable to certain kinds infections but not others.
Hyper IgE
IgA Deficiency
Isolated IgG Subclass Deficiency
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