What is the history of Erythromelalgia?

When was Erythromelalgia discovered? What is the story of this discovery? Was it coincidence or not?


Erythromelalgia is a rare neurovascular disorder characterized by episodes of intense burning pain, redness, and heat in the extremities, typically the hands and feet. The condition was first described in medical literature in the late 19th century, but its history can be traced back even further.



Early Observations:



The earliest known reference to symptoms resembling erythromelalgia dates back to the 16th century when French physician Ambroise Paré described a condition called "burning feet." However, it wasn't until the late 19th century that the disorder gained recognition as a distinct medical entity.



Discovery and Naming:



In 1878, French physician Maurice Raynaud first identified the condition and named it "erythromelalgia." He observed patients experiencing episodes of redness, heat, and pain in their extremities, which were exacerbated by warmth and relieved by cold. Raynaud's initial description laid the foundation for understanding the disorder.



Advancements in Understanding:



Throughout the 20th century, researchers made significant progress in unraveling the mechanisms and causes of erythromelalgia. In the 1930s, it was recognized as a distinct syndrome separate from Raynaud's disease. The condition was found to be associated with abnormalities in the peripheral nerves and blood vessels, leading to the characteristic symptoms.



Genetic Discoveries:



In recent years, genetic studies have shed light on the hereditary nature of erythromelalgia. In the early 2000s, mutations in the SCN9A gene were identified as a major cause of the disorder. The SCN9A gene encodes a sodium channel involved in transmitting pain signals. Mutations in this gene result in increased excitability of pain-sensing neurons, leading to the intense pain experienced by individuals with erythromelalgia.



Current Understanding and Treatment:



Today, erythromelalgia is recognized as a rare and chronic condition with no known cure. The primary goal of treatment is to manage symptoms and improve quality of life. Cooling measures, such as cold water soaks or ice packs, are often used to alleviate pain during episodes. Medications that target nerve excitability, such as sodium channel blockers, may also be prescribed.



Ongoing Research:



Research into erythromelalgia continues to advance our understanding of the disorder. Scientists are exploring additional genetic mutations associated with the condition and investigating potential new treatment options. The rarity of erythromelalgia poses challenges in conducting large-scale studies, but ongoing efforts aim to improve diagnosis, management, and ultimately find a cure.


by Diseasemaps

Silas Weir Mitchell discovered this disease in 1878. He came up with the word Erthromelalgia which would explain the redness and burning pain in the extremities.

9/16/17 by Jeff 3050

Originally called Mitchell Disease, after a researcher and doctor, now currently called Erythromelalgia. Found all over the world in all races and ages

12/27/17 by mleaver 2500

Sir Mitchell discovered the disease. Erythromelalgia is also known as Mitchell's disease because of this

4/4/18 by Alys 2500

In 1878 by Silas Mitchell I believe he was practicing in Pennsylvania and saw a number of people over time with red painful limbs. He is considered the father of neurology.

1/18/21 by Kathy Vanicek 2500

The term Erythromelalgia was coined in 1878 but that doesn’t mean it was the first time people found it. For years people only thought it was genetic. In 2008 a study of familial EM was done where only two of the people assessed were found to have the gene that’s commonly tested for. The two other genes did not show any markers in the rest of the patients. Long winded way of saying for all of its time being known to us, we know VERY LITTLE.

8/14/21 by saguaros 3000

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