References

Read on for a list of associations and organizations that provide helpful information, resources and support for people living with SM.

Read on to learn the answers to some of the most frequently asked questions (FAQs) about systemic mastocytosis.

Systemic mastocytosis can affect many organs and systems in the body, so various medical specialists must work together to care for patients.

Different therapies are available for patients with systemic mastocytosis (SM) based on the symptoms and disease subtype of each patient.

There is no cure for systemic mastocytosis (SM), and treatment options depend on the disease type and the severity of the symptoms.

Systemic mastocytosis (SM) is considered an incurable disease, and prognosis is dependent on the patient’s disease type.

The symptoms of systemic mastocytosis (SM) develop as a result of the release of chemicals from mast cells and vary by patient.

SM diagnosis includes a review of the patient’s symptoms and medical history in addition to several medical tests.

Systemic mastocytosis (SM) is a rare disease that is usually caused by a sporadic mutation in the KIT gene.

Find out what you need to know about systemic mastocytosis (SM), a rare hematological disease characterized by mast cells.