What does WHIM mean in BRITISH MEDICINE
WHIM Syndrome is a rare genetic disorder that affects both males and females. It is caused by an abnormal gene, which makes the body unable to make certain proteins needed to fight infections. People with WHIM Syndrome suffer from a number of immune-related symptoms, including warts, hypogammaglobulinemia, recurrent infections, and myelokathexis. The combination of these symptoms provides the acronym WHIM. In this article we will take a closer look at this condition and provide further information on its diagnosis and treatment options
WHIM meaning in British Medicine in Medical
WHIM mostly used in an acronym British Medicine in Category Medical that means warts, hypogammaglobulinemia, infections, myelokathexis, see WHIM syndrome
Shorthand: WHIM,
Full Form: warts, hypogammaglobulinemia, infections, myelokathexis, see WHIM syndrome
For more information of "warts, hypogammaglobulinemia, infections, myelokathexis, see WHIM syndrome", see the section below.
Symptoms
The primary symptom of WHIM Syndrome is intermittent warts on the hands and feet which can be painful and itchy. Many patients also experience recurrent infections such as common colds, ear infections and sinusitis; as well as more serious bacterial and fungal infections. Additionally, people with WHIM Syndrome often have low levels of immunoglobulin A (IgA) which is an antibody used by the body to fight infection. Lastly, leukocyte migration (myelokathexis) may be impaired in these individuals leading to increased risk of infection
Essential Questions and Answers on warts, hypogammaglobulinemia, infections, myelokathexis, see WHIM syndrome in "MEDICAL»BRITMEDICAL"
What is WHIM Syndrome?
WHIM Syndrome stands for Warts, Hypogammaglobulinemia, Infections and Myelokathexis; it is a rare, primary immunodeficiency disorder caused by a mutation in the CXCR4 gene.
What are the symptoms of WHIM Syndrome?
The most common symptoms of WHIM Syndrome include recurrent warts, infections, low immunity levels and myelokathexis — a deficiency in white blood cells.
Are there any treatments for WHIM Syndrome?
While there is no specific cure for WHIM Syndrome, treatment involves controlling and managing symptoms as well as boosting immune system function with medications such as G-CSF. Other treatments may also be recommended depending on the individual's needs.
How is WHIM Syndrome diagnosed?
Diagnosis of WHIM Syndrome typically involves genetic testing to check for mutations in the CXCR4 gene. Blood tests to measure antibody levels in the body can also help diagnose and confirm the presence of hypogammaglobulinemia.
Who is at risk of developing WHIM Syndrome?
Although anyone can develop WHIM Syndrome, it is estimated that 1 out of 1 million individuals worldwide have this condition and it appears to affect more males than females.
What other conditions might be associated with WHIM Syndrome?
While each person may experience different symptoms based on their own case, other health issues that may be associated with having WHIM Syndrome include skin rashes or lesions, chronic ear infections, sinusitis and pneumonia. In some cases autoimmune disorders such as juvenile arthritis may also be present.
Is there any way to prevent getting WHIM syndrome?
Since researchers believe that who has this condition inherit it from a parent carrying one mutated copy of a certain gene — meaning that it cannot be prevented— patients should talk to their doctors about available support systems and management options.
How does a person manage their daily life when suffering fromWHIM syndrome?
People living with WHIM syndrome should try to stay away from others who have highly contagious illnesses such as chickenpox or influenza while also receiving vaccinations against common illnesses like polio or measles. Additionally eating nutritious foods, maintaining regular exercise and staying completely up-to-date on all medications will help ensure quality-of-life.