Results 181 to 190 of about 3,196,729 (227)

Linear Scleroderma Associated With Progressive Brain Atrophy

Brain and Development, 2003
Linear scleroderma (LS) is characterized by scleroatrophic lesions affecting limbs and legs, unilaterally. Neurological involvement may be associated with ipsilateral facial and skull involvement in disorders referred to clinically as LS 'en coup de ...
Salvatore Grosso, Antonella Fioravanti, Giovanni Biasi   +2 more
exaly   +2 more sources

Melorheostosis: Report of a New Case With Linear Scleroderma

Clinical Rheumatology, 1998
Melorheostosis is a very rare bone disease of unknown etiology characterised by linear hyperostosis and associated with fibrosis of soft tissues and the skin.
M Birtane
exaly   +2 more sources

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Melorheostosis With Linear Scleroderma

Archives of Dermatology, 1963
The seventh case of linear scleroderma associated with melorheostosis is presented and the literature reviewed. Melorheostosis is a rare disorder of bone, first described in 1922. It is a peculiar, linear hyperostosis, usually in an extremity, that has been likened to the tallow drippings on the side of a burning candle.
S A, MULLER, E D, HENDERSON
openaire   +2 more sources

LINEAR MELORHEOSTOTIC SCLERODERMA

British Journal of Dermatology, 1972
Summary.— A case of melorheostosis with overlying skin changes is reported This skin lesion is best termed linear melorheostotic scleroderma to differen tiate it from true linear scleroderma. It is characterized by proliferation into the subcutaneous fat of normal-appearing collagen and elastic tissue in lobes and lobules producing an irregular ...
L T, Wagers, A W, Young, S F, Ryan
openaire   +2 more sources

Linear Scleroderma in Children

Archives of Pediatrics & Adolescent Medicine, 1981
• Two children with linear scleroderma (linear morphea) and similar clinical and serological findings were followed up for three years. One of the patients had been given penicillamine. The treated patient suffered atrophy of three extremities, whereas the untreated patient has had no progression of his disease. ( Am J Dis Child 1981;135:738-740)
R W, Kesler, T D, McDonald, M, Balasubramaniam, F T, Saulsbury   +3 more
openaire   +2 more sources

LINEAR SCLERODERMA IN CHILDREN

International Journal of Dermatology, 1996
Abstract Background. Linear scleroderma is a cutaneous disease of unknown etiology. It most often affects children, who develop band‐like lesions in an asymmetric distribution. The literature is reviewed as to the diagnosis, pathogenesis, and treatment of linear scleroderma. Case Report.
L E, Eubanks, E I, McBurney, W, Galen, R, Reed   +3 more
openaire   +2 more sources

Linear Scleroderma

Annals of Internal Medicine, 1986
The clinical features and natural history of linear scleroderma in 53 patients and the laboratory tests helpful in the management of this disease are described. No patient had Raynaud's phenomenon or signs of systemic connective tissue disease in a mean follow-up of 10 years.
V, Falanga, T A, Medsger, M, Reichlin, G P, Rodnan   +3 more
openaire   +2 more sources

Localized Linear Scleroderma with Cutaneous Calcinosis

The Journal of Dermatology, 2002
AbstractA 38‐year‐old woman developed sclerotic and atrophic changes of the left femur in the winter of 1976. In 1980, she was referred to our dermatology clinic and was diagnosed with localized linear scleroderma from the results of the physical examinations and the histological findings.
Ai, Yamamoto, Akimichi, Morita, Yoichi, Shintani, Shigeru, Sakakibara, Takuo, Tsuji   +4 more
openaire   +2 more sources

Topical calcipotriene for morphea/linear scleroderma

Journal of the American Academy of Dermatology, 1998
Morphea and linear scleroderma are characterized by erythema, induration, telangiectasia, and dyspigmentation. There is no universally effective treatment. Oral calcitriol has been beneficial in the treatment of localized and extensive morphea/scleroderma, but the use of topical calcipotriene has not been reported.The purpose of this study was to ...
B B, Cunningham, I D, Landells, C, Langman, D E, Sailer, A S, Paller   +4 more
openaire   +2 more sources

Childhood‐type myositis and linear scleroderma

Neurology, 1983
A 5-year-old girl had linear scleroderma on the flexor surface of the right arm; muscle wasting included the shoulder girdle. IgM fluorescence on blood vessels and along dermal-epidermal junction was observed by direct immunofluorescence in biopsied skin.
T, Miike, Y, Ohtani, S, Hattori, T, Ono, T, Kageshita, I, Matsuda   +5 more
openaire   +2 more sources