Glanzmann's diasease; Thrombasthenia - Glanzmann
Glanzmann disease is a rare disorder of blood platelets. Platelets are a part of the blood that aids in blood clotting.
Glanzmann disease is caused by the lack of a protein that is normally on the surface of platelets. This substance is needed for platelets to clump together to form blood clots.
The condition is congenital, which means it is present from birth. There are several genetic abnormalities that can cause the condition.
Symptoms may include any of the following:
- Heavy bleeding during and after surgery
- Bleeding gums
- Bruising easily
- Heavy menstrual bleeding
- Nosebleeds that do not stop easily
- Prolonged bleeding with minor injuries
Exams and Tests
The following tests may be used to diagnose this condition:
Other tests may be needed. Family members may also need to be tested.
There is no specific treatment for this disorder. Platelet transfusions may be given to people who are having severe bleeding.
Glanzmann disease is a lifelong condition, and there is no cure. You should take special steps to try to avoid bleeding if you have this condition.
Anyone with a bleeding disorder should avoid taking aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and naproxen. These drugs can prolong bleeding times by preventing platelets from clumping.
Complications may include:
When to Contact a Medical Professional
Call your health care provider if:
- You have bleeding or bruising of an unknown cause
- Bleeding does not stop after usual treatments
Glanzmann disease is an inherited condition. There is no known prevention.
Macartney CA, Paredes N, Chan AKC. Disorders of coagulation in the neonate. In: Hoffman R, Benz EJ Jr, Silberstein LE, Heslop HE, Weitz JI, Anastasi J, eds. Hematology: Basic Principles and Practice. 6th ed. Philadelphia, PA: Elsevier Saunders; 2013:chap 152.
Nichols WL. Von Willebrand disease and hemorrhagic abnormalities of platelet and vascular function. In: Goldman L, Schafer AI, eds. Goldman-Cecil Medicine. 25th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 173.