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polymyositis/muntah
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Multiple acyl-CoA dehydrogenation deficiency as decreased acyl-carnitine profile in serum.
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We report a case with late onset riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency (MADD) characterized by decreased acyl-carnitine profile in serum which is consistent with primary systemic carnitine deficiency (CDSP) while just the contrary to a typical MADD. This patient
Eosinophilic gastroenteritis associated with systemic lupus erythematosus.
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Eosinophilic gastroenteritis is an uncommon disease with an obscure etiology, although associations with allergy, the idiopathic hypereosinophilic syndrome, and connective tissue disease have been reported. We present the case of a 37-year-old woman with a history of idiopathic thrombocytopenic
Acute myopathy in a patient with oesophageal stricture.
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BACKGROUND
Muscle injury may be caused by any one of a number of factors, including trauma, drugs, hyperthermia and metabolic derangement. Symptoms and signs are often non-specific, and myopathy may be easily overlooked.
METHODS
An elderly woman was referred to hospital for investigation of rapidly
[Gastroenterologic aspects of connective tissue diseases].
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The connective tissue disorders are a protean group of acquired diseases which have in common widespread immunologic and inflammatory alterations of connective tissue. The acquired connective tissue diseases generally include the following clinical entities: rheumatoid arthritis, systemic lupus
Clinical and upper gastrointestinal motility features in systemic sclerosis and related disorders.
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OBJECTIVE
The aim of this study was to characterize the clinical and motility findings in 62 patients with systemic sclerosis or related disorders referred for evaluation of upper gastrointestinal (GI) symptoms.
METHODS
Methods included retrospective clinical record review and quantitation of
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