May-Hegglin Anomaly (MHA) is a rare genetic disorder that affects the blood and bone marrow. It is characterized by a triad of symptoms including thrombocytopenia (low platelet count), giant platelets, and white blood cell inclusions called Döhle-like bodies. While May-Hegglin Anomaly is the commonly used term to describe this condition, there are a few other synonyms that are sometimes used:
It is important to note that while these synonyms are sometimes used, May-Hegglin Anomaly remains the most commonly recognized and accepted term for this condition. If you or someone you know has been diagnosed with MHA, it is recommended to consult with a healthcare professional for accurate diagnosis, management, and support.