If you are living with a primary immunodeficiency (PID), including neutropenia, you and your doctors may have spent a lot of time—using trial and error—to understand your symptoms and possible treatments. You may have been misdiagnosed or even still feel that you haven’t found the right diagnosis.
Now, diagnostic genetic testing may give you answers and may also be a way to find a treatment that is more specific to your needs now or in the future, sometimes based on the specific type of mutation that is identified. Talk to your doctor to find out if genetic testing is an option for you.
People with neutropenia have a reduced number of neutrophils, a type of white blood cell. The lower the neutrophil count, the greater the risk of infection. Congenital neutropenia is both a rare blood disorder and a rare type of primary immunodeficiency (PID).
Neutropenia can also be described in three other ways: as a “subclass” of PID, as a “feature of” or as “associated with” a specific PID (like WHIM syndrome). People living with neutropenia may see a specialist (like a hematologist or immunologist) to treat their neutropenia. Not all specialists describe neutropenia the same way and not all describe it as a type of PID.
There are many ways to categorize neutropenia, which can make it even more confusing. Someone may be diagnosed with severe chronic neutropenia which can also be severe congenital neutropenia. You may be diagnosed with neutropenia but not know exactly what type you have. Or, you may not have been told about the neutropenia/PID link. A genetic test may be able to help you learn more about your neutropenia and your treatment options.
|Severity||Based on ANC (Absolute Neutrophil Count) blood test:|
Mild: ANC above 1000 per mm3
Moderate: ANC 500 per mm3 to 1000 per mm3
Severe: ANC < 500 per mm3 (0.5 x 109/l)
|Duration||Acute: temporary or short-lasting |
Chronic: long-lasting, neutropenia symptoms for more than 3 months
|Cyclic||Varying neutrophil counts with a typical cycle length of 21 days|
|Cause||Congenital: neutropenia that one is born with, runs in families or has a genetic cause|
Acquired: neutropenia that is caused by something else over a period of time
Idiopathic: neutropenia whose cause is unknown