Results 141 to 150 of about 19,449 (186)
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Annals of Internal Medicine, 1965
Excerpt In his classic review on Werner's syndrome published in the ANNALS in 1945, Thannhauser (1) was the first to define clearly the essential features of the syndrome and to distinguish it from...
T R, RILEY +3 more
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Excerpt In his classic review on Werner's syndrome published in the ANNALS in 1945, Thannhauser (1) was the first to define clearly the essential features of the syndrome and to distinguish it from...
T R, RILEY +3 more
openaire +4 more sources
The American Journal of Medicine, 1973
Abstract This is a report of a new case of Werner's syndrome. The clinical picture consisted of short stature, premature aging of the skin, bilateral cataracts, high-pitched voice, generalized subcutaneous and muscle atrophy, scleroderma-like plaques, gangrene, Monckeberg sclerosis and organic brain syndrome. Plasma lipids and lipoprotein pattern were
R, Fleischmajer, A, Nedwich
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Abstract This is a report of a new case of Werner's syndrome. The clinical picture consisted of short stature, premature aging of the skin, bilateral cataracts, high-pitched voice, generalized subcutaneous and muscle atrophy, scleroderma-like plaques, gangrene, Monckeberg sclerosis and organic brain syndrome. Plasma lipids and lipoprotein pattern were
R, Fleischmajer, A, Nedwich
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Archives of Internal Medicine, 1952
ORIGINALLY believed to be an excessively rare heredofamilial disorder, Werner's syndrome has been recognized with increasing frequency in recent years. The syndrome is featured by the unique combination of physical immaturity, early senescence, premature cataracts, scleroderma-like skin changes, and a tendency toward development of diabetes mellitus ...
H, BOATWRIGHT, C E, WHEELER, E P, CAWLEY
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ORIGINALLY believed to be an excessively rare heredofamilial disorder, Werner's syndrome has been recognized with increasing frequency in recent years. The syndrome is featured by the unique combination of physical immaturity, early senescence, premature cataracts, scleroderma-like skin changes, and a tendency toward development of diabetes mellitus ...
H, BOATWRIGHT, C E, WHEELER, E P, CAWLEY
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Australian and New Zealand Journal of Medicine, 1977
A case of Werner syndrome is reported. The patient was prematurely old, had skin atrophy, characteristic posterior subcapsular cataracts and prepubertal primary hypogonadism. Additional ocular features compatible with premature ageing included presbyopia, arcus seniles and diminished tear flow.
S K, Samantray +3 more
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A case of Werner syndrome is reported. The patient was prematurely old, had skin atrophy, characteristic posterior subcapsular cataracts and prepubertal primary hypogonadism. Additional ocular features compatible with premature ageing included presbyopia, arcus seniles and diminished tear flow.
S K, Samantray +3 more
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Werner’s Syndrome and Astrocytoma
Dermatologica, 2009Werner’s syndrome, a relatively rare and autosomal recessive disorder, is well known to be characterized by a high frequency of malignant neoplasms. Werner’s syndrome has not infrequently been associated with meningiomas. We report a case of Werner’s syndrome and temporal astrocytoma in a 49-year-old male.
F J, Laso +4 more
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Werner's syndrome as “Hyaluronuria”
Clinica Chimica Acta, 1975Abstract Although excretion of acid glycosaminoglycans into urine of five patients with Werner's syndrome were within normal limits, the quantity of hyaluronic acid increased in this disease. To this novel finding, a term “Hyaluronuria” was proposed.
M, Tokunaga +4 more
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Pathology of the Werner Syndrome
1985Anatomic-pathological observation remains one of the fundamental approaches to the understanding of multiple system disease of unknown etiology. In this paper, we review the results of such anatomic investigations of necropsies of subjects with the Werner syndrome, including five cases (all Japanese subjects) that we have personally autopsied, one of ...
T, Ishii +5 more
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Dermatologica, 2009
The symptoms of Werner’s Syndrome are reported by means of 2 cases. The importance of an endocrinological and ophthalmological examination of patients with ‘systemic sclerosis’ is demonstrated.
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The symptoms of Werner’s Syndrome are reported by means of 2 cases. The importance of an endocrinological and ophthalmological examination of patients with ‘systemic sclerosis’ is demonstrated.
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Archives of Ophthalmology, 1974
To the Editor. —In the July issue of theArchives(90:53-56, 1973), Drs. Bullock and Howard reported a case of Werner syndrome. I find the diagnosis unconvincing because of the number of atypical features, which are as follows: Age of presentation. Cataract is commonly present by the age of 20, and by the age of 30 causes severe visual impairment.
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To the Editor. —In the July issue of theArchives(90:53-56, 1973), Drs. Bullock and Howard reported a case of Werner syndrome. I find the diagnosis unconvincing because of the number of atypical features, which are as follows: Age of presentation. Cataract is commonly present by the age of 20, and by the age of 30 causes severe visual impairment.
openaire +2 more sources