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IMMUNODEFICIENCY
GROUP 3
OUTLINE
History
What is Immunodeficiency
Types of Immunodeficiency
Deficiencies under types
Allergies
INTRODUCTION
This condition that was initially coined as swiss
type agammaglobulinemia was renamed as severe
combined immunodeficiency (SCID) by world
health organization (WHO) in 1970. In 1954,
Robert Good discovered a fatal granulomatous
disease that is now known as chronic
granulomatous disease (CGD).
WHAT IS IMMUNODEFICIENCY?
It is the absence or failure of normal function of one or
more elements of the immune system
Results in immunodeficiency disease
Can be specific or non specific
Specific = Abnormalities of B & T cells
Non specific = Abnormalities of non specific components
IMMUNODEFICIENCY
There are types of immunodeficiency's;
Primary immune deficiency
Secondary immune deficiency
PRIMARY IMMUNE DEFICIENCY
These are diseases that are caused by inherited genetic
mutations
These inherited genetic mutations may be in specific or non
specific immune mechanisms
They weaken the immune system allowing infections and
other health problems to occur more easily
They can also be called Congenital Immunodeficiency's
Example are;
X-linked agammaglobulinemia(XLA)
Common variable immunodeficiency(CVID)
Severe combined immunodeficiency(SCID)
SECONDARY IMMUNE DEFICIENCY
A secondary immune deficiency disease occurs when the
immune system is comprised due to an environment factor.
Examples of these outside forces include HIV,
chemotherapy, severe burns or malnutrition.
Secondary immunodeficiency's also known as acquired
immunodeficiency's, can result from many
immunosuppressive agent, for example, malnutrition, aging,
particular medications.
Examples are:
AIDS
Leukemia
SIGNS AND SYMPTOMS
Pinkeye
Sinus infections
Colds
Diarrhea
Yeast infection
Pneumonia
CAUSES
Causes of the immunodeficiency may vary
depending on the nature of the disorder
The cause may be either genetic or acquired by
malnutrition and poor sanitary conditions
TREATMENT
Treatment of immunodeficiency can be grouped
into two which is;
Treating the infections
Infections must be treated with antibiotics
Boosting the immune system
Using of vaccines
RISK FACTORS
The only known risk factor is having a family
history of a primary immune deficiency disorder,
which increases your risk of having the condition.
If you have a type of the condition, you might want
to seek genetic counselling if you plan to have a
family.
COMPLICATIONS
Complications caused by a primary immunodeficiency
disorder vary, depending on what type you have. They can
include:
Recurrent infections
Autoimmune disorders
Damage to heart, lungs, nervous system or digestive tract.
Slowed growth
Increased risk of cancer
Death from serious infection
REFERENCES
Chinen, J and Shearer, W.( 2010)
Secondary Immunodeficiencies, including HIV
infections, journal of Allergy and Clinical
Immunology, 125(2),pp.195-203
Immunodeficiency by Dr. Saul Greenberg.
Univerity of Toronto. Last updated, on February 5,
2009.

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Immunodeficiency group 3

  • 2. OUTLINE History What is Immunodeficiency Types of Immunodeficiency Deficiencies under types Allergies
  • 3. INTRODUCTION This condition that was initially coined as swiss type agammaglobulinemia was renamed as severe combined immunodeficiency (SCID) by world health organization (WHO) in 1970. In 1954, Robert Good discovered a fatal granulomatous disease that is now known as chronic granulomatous disease (CGD).
  • 4. WHAT IS IMMUNODEFICIENCY? It is the absence or failure of normal function of one or more elements of the immune system Results in immunodeficiency disease Can be specific or non specific Specific = Abnormalities of B & T cells Non specific = Abnormalities of non specific components
  • 5. IMMUNODEFICIENCY There are types of immunodeficiency's; Primary immune deficiency Secondary immune deficiency
  • 6. PRIMARY IMMUNE DEFICIENCY These are diseases that are caused by inherited genetic mutations These inherited genetic mutations may be in specific or non specific immune mechanisms They weaken the immune system allowing infections and other health problems to occur more easily They can also be called Congenital Immunodeficiency's Example are; X-linked agammaglobulinemia(XLA) Common variable immunodeficiency(CVID) Severe combined immunodeficiency(SCID)
  • 7. SECONDARY IMMUNE DEFICIENCY A secondary immune deficiency disease occurs when the immune system is comprised due to an environment factor. Examples of these outside forces include HIV, chemotherapy, severe burns or malnutrition. Secondary immunodeficiency's also known as acquired immunodeficiency's, can result from many immunosuppressive agent, for example, malnutrition, aging, particular medications. Examples are: AIDS Leukemia
  • 8. SIGNS AND SYMPTOMS Pinkeye Sinus infections Colds Diarrhea Yeast infection Pneumonia
  • 9. CAUSES Causes of the immunodeficiency may vary depending on the nature of the disorder The cause may be either genetic or acquired by malnutrition and poor sanitary conditions
  • 10. TREATMENT Treatment of immunodeficiency can be grouped into two which is; Treating the infections Infections must be treated with antibiotics Boosting the immune system Using of vaccines
  • 11. RISK FACTORS The only known risk factor is having a family history of a primary immune deficiency disorder, which increases your risk of having the condition. If you have a type of the condition, you might want to seek genetic counselling if you plan to have a family.
  • 12. COMPLICATIONS Complications caused by a primary immunodeficiency disorder vary, depending on what type you have. They can include: Recurrent infections Autoimmune disorders Damage to heart, lungs, nervous system or digestive tract. Slowed growth Increased risk of cancer Death from serious infection
  • 13. REFERENCES Chinen, J and Shearer, W.( 2010) Secondary Immunodeficiencies, including HIV infections, journal of Allergy and Clinical Immunology, 125(2),pp.195-203 Immunodeficiency by Dr. Saul Greenberg. Univerity of Toronto. Last updated, on February 5, 2009.