Types of PI

Primary Immunodeficiency (PI) is an umbrella term for over 250 genetic defects and disorders of the immune system recognized by the World Health Organization. Together they affect approximately 29,000 Canadians. Primary Immunodeficiency is not considered a rare disease as a category, but each individual form of PI is rare.

We are currently developing a detailed list of disorders under the umbrella of PI. Disorders will be arranged in alphabetical order and are searchable.

All | # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
There are currently 3 names in this directory
Adenosine deaminase deficiency (also called ADA deficiency or ADA-SCID) is an autosomal recessive metabolic disorder that causes immunodeficiency. It occurs in fewer than one in 100,000 live births worldwide. It accounts for about 15% of all cases of severe combined immunodeficiency (SCID). ADA-SCID is a rare disease in which patients cannot make lymphocytes (a type of white blood cell) and, as a result, have a severely deficient immune system. A faulty gene inherited from both parents stops production of an essential protein called adenosine deaminase (ADA), which is particularly important for the formation of lymphocytes and a functioning immune system. Children born with ADA-SCID have an impaired ability to fight off everyday infections resulting in severe and life-threatening illness. They rarely survive beyond 1-2 years unless immune function is restored. Patients with ADA-SCID initially take antibiotics and antifungal treatments to help protect themselves from serious infections, but most require a bone marrow transplant from a matched donor. However, the effectiveness of these transplants is highly dependent upon how close the match is between donor and patient. If no suitable donors are available, gene therapy, if approved, will provide another option. Credits: Immune Deficiency FoundationGenetics Home Reference

Antibody Deficiency with Normal/Elevated Immunoglobulins
This one of the various antibody deficiency disorders. Individuals with antibody deficiencies tend to get upper respiratory infections or infections of the sinuses or lungs (eg. streptococcus pneumonia, hemophilus influenzae). Those with Antibody Deficiency with Normal/Elevated Immunoglobulins have severe infections similar to patients with Common Variable Immunodeficiency (CVID), but their immunoglobulin levels are normal/elevated. Credits: Immune Deficiency Foundation

Ataxia-Telangiectasia (A-T) is a condition that affects multiple body systems. People with A-T have an unsteady, wobbly gait (ataxia) which worsens with age. Typically, they require a wheelchair for mobility by adolescence. Individuals with A-T have dilated, corkscrew-shaped blood vessels called "telangiectasia" on the whites of the eyes and certain areas of skin. A major symptom is a deficient immune system, often making those with A-T susceptible to lung infections. Individuals with A-T also have higher chances of getting cancer, particularly lymphoma and leukaemia. The condition occurs in 1 in 40,000 to 100,000 people worldwide. Credits: Immune Deficiency FoundationGenetics Home Reference
  • Language

  • Cornerstone Club