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Dripping Candle Wax Bone Disease (Melorheostosis) Cause Solved

Published: 2018-04-13
Author: NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases | Contact:

Synopsis: National Institutes of Health research study finds gene mutations that cause Melorheostosis or dripping candle wax bone disease.

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NIH researchers crack mystery behind rare bone disorder - Study finds gene mutations that cause 'dripping candle wax' bone disease...


Melorheostosis, also known as Leri disease, is an uncommon mesenchymal dysplasia manifesting as regions of sclerosing bone with a characteristic dripping or flowing candle wax appearance. Melorheostosis tends to be limited to one extremity. Melorheostosis often affects the lower limbs, although it can affect the arms or hands as well. Rarely it affects the spinal column, skull, or ribs. It most often affects just one area of the body, but rarely can affect multiple areas. The disorder is progressive, with the ultimate severity of symptoms often depending on age of onset. In severe cases amputation has been performed when conservative measures such as physical therapy and regional anesthetics have been ineffective.

An x-ray image of a patient with melorheostosis shows excess bone formation, likened to dripping candle wax - Image Credit: U.S. National Institutes of Health (NIH).
An x-ray image of a patient with melorheostosis shows excess bone formation, likened to dripping candle wax - Image Credit: U.S. National Institutes of Health (NIH).

Researchers at the National Institutes of Health worked with 15 patients from around the world to uncover a genetic basis of "dripping candle wax" bone disease. The rare disorder, known as melorheostosis, causes excess bone formation that resembles dripping candle wax on x-rays. The results, appearing in Nature Communications, offer potential treatment targets for this rare disease, provide important clues about bone development, and may lead to insights about fracture healing and osteoporosis.

Though there are only about 400 known cases of this disorder worldwide, 15 unrelated adults with the condition from around the globe volunteered to come to the NIH Clinical Center to undergo biopsies of both affected and unaffected bones. The condition causes pain and bone deformity, which can limit the function of bones.

"Scientists previously assumed that the genetic mutations responsible for melorheostosis occurred in all cells of a person with the disorder," said co-senior author Timothy Bhattacharyya, M.D., head of the Clinical and Investigative Orthopaedics Surgery Unit at the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) at NIH. "Our team hypothesized that mutations might only occur in the affected bone tissue."

Researchers compared samples of healthy and affected bone from each participant to look for differences in the exome, the portion of the genome that codes for proteins. Comparing genetic information from both samples in each patient allowed the team to pinpoint even low levels of the mutations. Experts from NIAMS and the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) worked together on this study.

The analysis revealed that 8 of the 15 participants had mutations in the MAP2K1 gene in the affected bone only. MAP2K1 produces the protein MEK1. The gene MAP2K1 has previously been linked to some types of cancerous growths as well as to conditions that lead to abnormal blood vessel formation in the head, face or neck.

In melorheostosis, all the identified MAP2K1 mutations affect a region of the MEK1 protein that normally suppresses its activity, thus they cause MEK1 to become overactive. The bone growth is considered benign and does not spread to other parts of the body.

"This is an exciting study of a very rare bone disorder that not only identified the responsible mutation in half of the patients, but uncovered fundamental information about the role of a cancer-related gene in the metabolic pathways of normal bone," said study co-senior author Joan Marini, Ph.D., M.D., of NICHD. "When we started, we had no preconceived causative pathways, but the participation of the patients has really changed the scientific landscape on this topic. Further studies on how this pathway works in both normal and mutant bone cells may have broad implications that could benefit a wider population."

"Most adults have the problem of weakening bones as they grow older. These patients have the opposite problem as some of their bones are rock hard and still growing," said Bhattacharyya. "The prospect that we could somehow harness this pathway in the future is so exciting."

The study was supported by the NIH Intramural Research Program (ZIDAR041180 and Z1AHD000408) and the Melorheostosis Association. The Ludwig Boltzmann Institute of Osteology in Austria worked with the NIH on this study.

The study is registered at as NCT02504879.

Bhattacharyya T, Marini JC et al. Somatic activating mutations in MAP2K1 cause melorheostosis (link is external). Nature Comms. 2018 Apr 11. doi:10.1038/s41467-018-03720-z

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Cite This Page (APA): NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases. (2018, April 13). Dripping Candle Wax Bone Disease (Melorheostosis) Cause Solved. Disabled World. Retrieved January 16, 2022 from