Gingival capillary changes and oral motor weakness in juvenile dermatomyositis

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Gingival capillary changes and oral motor weakness in juvenile dermatomyositis.

OBJECTIVE We assessed the orofacial involvement in JDM, and evaluated the possible association of gingival and mandibular mobility alterations with demographic data, periodontal indices, clinical features, muscle enzyme levels, JDM scores and treatment. METHODS Twenty-six JDM patients were studied and compared with 22 healthy controls. Orofacial evaluation included clinical features, dental a...

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Association of nailfold capillary changes with disease activity, clinical and laboratory findings in patients with dermatomyositis

Background: The present study aimed to investigate the Nailfold Capillaroscopy (NC) features of the patients with dermatomyositis (DM) and its correlation with their disease activity indices, physical findings, and laboratory results. Methods: The present cross-sectional study was conducted on 27 DM patients above 16 years old who had referred to an(there are 3 clinics not one) outpatient rh...

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Gingival telangiectases: an underappreciated physical sign of juvenile dermatomyositis.

BACKGROUND MEDLINE searches (1966-June 1969) failed to identify references that give detailed descriptions of the oral manifestations of dermatomyositis (DM). However, several reports predating MEDLINE provided more complete descriptions of oral lesions associated with DM. OBSERVATIONS We describe 5 cases of juvenile DM with oral manifestations, primarily in the form of gingival telangiectase...

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Juvenile dermatomyositis.

Juvenile dermatomyositis (JDMS) is a chronic inflammatory condition characterized by muscle weakness and a distinctive rash caused by underlying vasculopathy. Long-term complications include subcutaneous and muscular calcification, contractures and in some cases the gradual development of a second connective tissue disease. Early aggressive treatment with systemic immunosuppressants and other a...

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Juvenile dermatomyositis.

The clinical profile of 7 children and their follow-up is described. There was female preponderance with mate to female ratio of 1:6. The median age of onset was 6 years. All the patients had skin rash, muscle weakness and abnormal enzyme profile. Muscle biopsy was performed in 6 and was abnormal in all of them. The electromyogram (EMG) was performed in 6 and was found abnormal in five. All the...

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ژورنال

عنوان ژورنال: Rheumatology

سال: 2010

ISSN: 1462-0324,1462-0332

DOI: 10.1093/rheumatology/keq189