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A rare case of melorheostosis of the hand in a pediatric patient
被引:2
|作者:
Willacy, Rolanda A.
[1
,2
,3
]
Clemmons, James A.
[1
]
Oyetan, Ore
[1
]
Khaleel, Ibrahim M.
[1
]
Salib, Christopher G.
[2
]
Wilson, Robert H.
[1
,2
,3
]
机构:
[1] Howard Univ, Coll Med, 520 W St NW, Washington, DC 20059 USA
[2] Howard Univ Hosp, Dept Orthoped Surg & Rehabil, 2401 Georgia Ave NW Suite 4300, Washington, DC 20060 USA
[3] Childrens Natl Hlth Syst, Div Orthoped Surg & Sports Med, 111 Michigan Ave NW, Washington, DC 20010 USA
关键词:
Melorheostosis;
Hyperostosis;
MAPK21;
oncogene;
Mesenchymal dysplasia;
Candle wax appearance;
Contractures;
LEMD3;
gene;
D O I:
10.1016/j.jor.2019.06.023
中图分类号:
R826.8 [整形外科学];
R782.2 [口腔颌面部整形外科学];
R726.2 [小儿整形外科学];
R62 [整形外科学(修复外科学)];
学科分类号:
摘要:
Melorheostosis, a rare mesenchymal dysplasia of bone, generally affects about 0.001% of people globally with about 400 cases total being reported. Melorheostosis of the hand, especially in the pediatric population, has been seldom reported. Previous studies have investigated potential genetic mutations associated with melorheostosis however, questions still remain regarding effective treatment options for this disease. This case report describes a unique case of pediatric melorheostosis of the hand and further clarifies current theories on melorheostosis with regards to pathogenesis, best treatment practices, and future research.
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页码:451 / 453
页数:3
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