Results 141 to 150 of about 3,066 (177)
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Melorheostosis With Scleroderma
Clinical Imaging, 2004The association of linear scleroderma with melorheostosis is very rare. Until now, only a few cases have been reported in the English literature. We describe a case of melorheostosis of a rib associated with overlying skin changes.
G, Shivanand, D N, Srivastava
exaly +3 more sources
Clinical Imaging, 2002 Melorheostosis is a rare bone disease of unknown etiology. It is characterized by tense and erythematous skin, contractures and shortening of the affected limbs.
Rocı́o P. Mariaud-Schmidt +3 more
core +4 more sources
Hide and Seek: Somatic SMAD3 Mutations in Melorheostosis
Journal of Experimental Medicine, 2020 : In the current issue of JEM, Kang et al. (https://doi.org/10.1084/jem.20191499) describe somatic mutations in the SMAD3 gene causing endosteal melorheostosis.
Joe Davis Velchev +2 more
exaly +2 more sources
Journal of Hand Surgery, 1996
We report a case of melorheostosis of the hand which showed a sclerotomal pattern of involvement, with swelling and pain. Surgical debulking resulted in correction of the deformity and relief of pain.
R, Sharma, F D, Burke
openaire +2 more sources
We report a case of melorheostosis of the hand which showed a sclerotomal pattern of involvement, with swelling and pain. Surgical debulking resulted in correction of the deformity and relief of pain.
R, Sharma, F D, Burke
openaire +2 more sources
Journal of Computer Assisted Tomography, 2008
Melorheostosis is a rare benign disease of cortical bone most frequently presenting as peripheral hyperostosis with a characteristic "melting wax" appearance on conventional radiographs. The disease most frequently affects the appendicular skeleton and is seen only rarely in the craniofacial bones.
Meredith, McDermott +2 more
openaire +2 more sources
Melorheostosis is a rare benign disease of cortical bone most frequently presenting as peripheral hyperostosis with a characteristic "melting wax" appearance on conventional radiographs. The disease most frequently affects the appendicular skeleton and is seen only rarely in the craniofacial bones.
Meredith, McDermott +2 more
openaire +2 more sources
Clinical Genetics, 2009 Mutations in the LEMD3 gene were recently incriminated in Buschke-Ollendorff syndrome (BOS) and osteopoikilosis, with or without melorheostosis. The relationship of this gene with isolated sporadic melorheostosis is less clear. We investigated LEMD3 in a
Marco Castori, M Paradisi, Bp Wordsworth
exaly +2 more sources
The Journal of Bone & Joint Surgery, 1950
The case reported is characteristic of melorheostosis in that the lesions were confined to the right upper extremity. The clinical course, with gradual progression and increasing pain, is also typical. Treatment by thoracic sympathectomy gave dramatic relief from symptoms.
W E, HESS, D M, STREET
openaire +2 more sources
The case reported is characteristic of melorheostosis in that the lesions were confined to the right upper extremity. The clinical course, with gradual progression and increasing pain, is also typical. Treatment by thoracic sympathectomy gave dramatic relief from symptoms.
W E, HESS, D M, STREET
openaire +2 more sources
Beitrage zur Orthopadie und Traumatologie, 1977
Melorheostosis is a seemingly rare condition of unknown etiology. Although it affects bone primarily, it may also involve soft tissue. The lower extremities are most frequently affected, and joints may become stiff as a result of obstruction of joint motion by thickened cortical sclerosis. The disease is difficult to diagnose in the early stages before
J, Krauss, H G, Baars
openaire +3 more sources
Melorheostosis is a seemingly rare condition of unknown etiology. Although it affects bone primarily, it may also involve soft tissue. The lower extremities are most frequently affected, and joints may become stiff as a result of obstruction of joint motion by thickened cortical sclerosis. The disease is difficult to diagnose in the early stages before
J, Krauss, H G, Baars
openaire +3 more sources