Diffuse Sclerosis
نویسندگان
چکیده
منابع مشابه
Diffuse endomyocardial sclerosis.
In recent years increasing attention has been focused upon a group of cases of congestive cardiac failure that present a distinctive cardiac morphology. There is diffuse thickening of the mural endocardium of one or both ventricles and fibrosis of the myocardium which is largely confined to the inner third of the ventricular wall; the coronary arteries are normal or show minimal arteriosclerosi...
متن کاملAdrenocortical atrophy and diffuse cerebral sclerosis.
Forsyth, C. C., Forbes, M., and Cumings, J. N. (1971). Archives of Disease in Childhood, 46, 273. Adrenocortical atrophy and diffuse cerebral sclerosis. A boy, diagnosed as having Addison's disease due to idiopathic atrophy of the adrenal glands at the age of 7 years, developed the first evidence of what was originally thought to be 'Schilder's disease' at 8 years and 10 months. He died at 9 ye...
متن کاملAddison's disease and diffuse cerebral sclerosis.
The rare combination of Addison's disease and diffuse cerebral sclerosis is now recognized to be something more than coincidence. Although only a small number of cases have been reported up to date, those cases have all followed a very similar pattern. This paper presents the case of a patient who is still alive and in whom, therefore, the diagnosis of diffuse cerebral sclerosis has not been co...
متن کاملA Case Report of Small Cell Lung Carcinoma in a Patient with Progressive Diffuse Sclerosis
Connective tissue diseases, including scleroderma, may be associated with an increased risk of lung cancer. The most common type of lung cancer associated with systemic sclerosis is adenocarcinoma or bronchoalveolar carcinoma, and small cell carcinoma is rare. This reports presents a 54-year-old non-smoker woman with a history of scleroderma who was examined due to aggravation of shortness of ...
متن کاملTwo Cases of Isolated Diffuse Mesangial Sclerosis with WT1 Mutations
Here we report two cases of isolated diffuse mesangial sclerosis (IDMS) with early onset end-stage renal failure. These female patients did not show abnormalities of the gonads or external genitalia. Direct sequencing of WT1 PCR products from genomic DNA identified WT1 mutations in exons 8 (366 Arg>His) and 9 (396 Asp>Tyr). These mutations have been reported previously in association with Denys...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1937
ISSN: 0035-9157
DOI: 10.1177/003591573703000801