Stiff person syndrome as the initial manifestation of systemic lupus erythematosus.

Y. Chronic inflammatory demyelinating polyneuropathy followed by systemic lupus erythematosus and Sjögren syndrome: a case report. Two cases of chronic inflammatory demyelinating polyradiculo-neuropathy (CIDP) associated with Graves' disease. The association of myasthenia gravis and connective tissue diseases-the role of Sjögren's syndrome. features of patients with myasthenia gravis associated with auto-immune diseases. of myasthenia gravis associated with systemic lupus erythemato-sus and pemphigus erythematosus. Myasthenic syndrome associated with sar-coidosis.thenic syndrome associated with Sjögren's syndrome and dis-coid lupus erythematosus. A close look at autoimmune muscle disorders: association of Lambert-Eaton myasthenic syndrome with dermatomyo-sitis.ated autoimmune diseases in patients with the Lambert-Eaton myasthenic syndrome and their families. A case of Addison's disease associated with the Lambert-Eaton myasthenic syndrome. syndrome associated with idiopathic thrombocytopenic purpura and diffuse panbronchiolitis: long-term remission after a course of intravenous immunoglobulin combined with low-dose pred-nisolone.Eaton myasthenic syndrome associated with minimal-change glomerulonephritis and psoriatic arthritis. Sydenham's chorea without evidence of rheumatic fever: report of its association with the Henoch-Schonlein syndrome and with systemic lupus erythematosus, and review of the literature. Video Fragile X-associated tremor/ataxia syndrome (FXTAS) is a neurodegenerative disorder that can affect carriers of a pre-mutation in the fragile X mental retardation 1 (FMR1) gene. 1 This gene normally contains fewer than 55 CGG triplet repeats. The full mutation (repeat number >200) is responsible for fragile X syndrome. Repeat lengths between 55 and 200 constitute a premutation which, besides being associated with FXTAS, also carries an increased risk of primary ovar-ian insufficiency (POI). 2,3 Symptoms of FXTAS usually begin in the seventh decade. Major motor abnormalities are action tremor, cerebellar ataxia affecting limbs and gait, and Parkinsonism. Other possible features include cognitive decline, neuropathy, and autonomic dysfunction. 4 The full phenotypic spectrum of FXTAS remains unclear. Although a broad range of neurological findings have been reported, 4 Additional supporting information may be found in the online version of this article. myoclonus has not previously been described in association with this syndrome. We describe a man with FXTAS who, besides known features of this syndrome, also has generalized reflex myoclonus. A 60-year-old man presented with a 2-year history of mild gait and balance difficulties. Past medical history consisted of treated hypertension and prostate cancer. Family history was notable for two sisters who experienced ovarian failure before age 35, and for the absence of mental retardation, par-kinsonism, tremor, ataxia, or dementia. Examination revealed mild memory impairment (Mini Mental State Examination score 28 out …