Clinical characteristics of 10 Chinese patients with melorheostosis and identification of a somatic MAP2K1 variant in one case Article Swipe
Xiaojun Han
,
Yang Xu
,
Zhanying Wei
,
Chun Wang
,
Hua Yue
,
Zhenlin Zhang
·
YOU?
·
· 2022
· Open Access
·
· DOI: https://doi.org/10.1002/mgg3.2043
YOU?
·
· 2022
· Open Access
·
· DOI: https://doi.org/10.1002/mgg3.2043
Background Melorheostosis (MEL) is an exceptionally rare sclerosing bone dysplasia with asymmetrically exuberant bone formation and soft tissue lesions in a segmental distribution. We aimed to summarize the clinical characteristics of Chinese MEL patients and identify their pathogenic cause. Methods In total, 10 Chinese MEL patients were recruited, and clinical manifestations and radiological characteristics were recorded. Sanger sequencing of the LEMD3 gene was performed on peripheral blood samples of all patients, while the exome sequencing of matched peripheral blood, melorheostotic bone, and skin lesion samples was conducted on one patient who provided affected bone and skin tissues. Micro‐computed tomography (micro‐CT) was also used to scan the melorheostotic bone tissue. Results We found the average age of the 10 MEL patients was 29.5 years (range 11–40 years), and the major symptoms were bone pain, restricted movement, and bone deformity. The lesions sites were mainly located in femur (8/10), tibia (8/10), fibula (6/10), and foot (7/10), the next was pelvis (4/10), and the last were patella (1/10), hand (1/10) and spine (1/10). Radiological examinations showed a mixture of hyperostosis consisting of classic “dripping candle wax,” “osteoma‐like,” or “myositis ossificans‐like” patterns in most patients. No germline pathogenic variants in the LEMD3 gene were found in all patients, but a disease‐causing somatic variant of MAP2K1 (c.167A > C, p.Gln56Pro) was detected in melorheostotic bone from one patient. Moreover, the micro‐CT analysis showed increased porosity in the melorheostotic bone with somatic MAP2K1 variant. Conclusion This is a summary of the clinical characteristics of Chinese MEL patients and we first identify the somatic MAP2K1 variant in Chinese patients. Our findings validate the molecular genetic mechanism of MEL and broaden its phenotype spectrum in the Chinese population.
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https://doi.org/10.1002/mgg3.2043Digital Object Identifier
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Clinical characteristics of 10 Chinese patients with melorheostosis and identification of a somatic MAP2K1 variant in one caseWork title
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articleOpenAlex work type
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enPrimary language
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2022Year of publication
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2022-08-25Full publication date if available
- Authors
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Xiaojun Han, Yang Xu, Zhanying Wei, Chun Wang, Hua Yue, Zhenlin ZhangList of authors in order
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https://doi.org/10.1002/mgg3.2043Publisher landing page
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YesWhether a free full text is available
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goldOpen access status per OpenAlex
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https://doi.org/10.1002/mgg3.2043Direct OA link when available
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Medicine, Pathology, Hyperostosis, Soft tissue, AnatomyTop concepts (fields/topics) attached by OpenAlex
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4Total citation count in OpenAlex
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2025: 1, 2024: 2, 2022: 1Per-year citation counts (last 5 years)
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