Werner’s syndrome: An underdiagnosed disorder resembling premature aging

Author:

Tollefsbol Trygve O.,Cohen Harvey Jay

Publisher

Springer Science and Business Media LLC

Subject

Geriatrics and Gerontology,Aging,General Medicine

Reference71 articles.

1. Werner, O.: Uber kataract in verbindung mit sklerodermie. Doctoral Dissertation, Kiel University. Schmidt and Klaunig, Kiel, 1904.

2. Oppenheimer, B.S. and Kugel, V.H.: Werner’s syndrome: Heredofamilial disorders with scleroderma, bilateral juvenile cataract, precocious graying of the hair and endocrine stigmatization. Trans. Assoc. Am. Physicians, 49: 358–370, 1934.

3. Thannhauser, S.J.: Werner’s syndrome (progeria of adults) and Rothmund sundrome: 2 types of closely related heredofamilial atrophic dermatoses with juvenile cataracts and endocrine features: Critical study of 5 new cases. Ann. Intern. Med., 23: 559–626, 1945.

4. Epstein, C.J., Martin, G.M., Schultz, A.L., and Motulsky, A.G.: Werner’s syndrome. A review of its symptomatology, natural history, pathologic features, genetics and relationships to the natural aging process. Medicine, 45: 177–221, 1966.

5. Martin, G.M.: Genetic syndromes in man with potential relevance to the pathobiology of aging. Birth Defects, 14: 5–39, 1978.

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