Literature DB >> 7357890

Werner's syndrome.

J A Zalla.   

Abstract

A typical patient with this uncommon premature aging syndrome was followed over a period of four and a half years until his death. He presented the characteristic clinical features, as well as the complications, of Werner's syndrome. About one hundred forty cases of this recessively inherited syndrome have been reported. Most patients become recognizable in their thirties by their short stature, typical facies, premature graying, hair loss, cataracts, atrophy of skin and subcutaneous tissue, and acral sclerosis. Advanced peripheral vascular disease occurs early; angina, skin cancer, diabetes mellitus, and internal malignancy are common. Most patients die before the age of fifty years either from complications of anteriosclerotic vascular disease or malignancy.

Entities:  

Mesh:

Year:  1980        PMID: 7357890

Source DB:  PubMed          Journal:  Cutis        ISSN: 0011-4162


  2 in total

Review 1.  Werner's syndrome: a review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations.

Authors:  D Salk
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

2.  High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency.

Authors:  D Cerimele; F Cottoni; S Scappaticci; G Rabbiosi; G Borroni; E Sanna; G Zei; M Fraccaro
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

  2 in total

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