Literature DB >> 7367844

[The Werner syndrome].

T Gottesmann, L Zala, A Vogel, M Mumenthaler.   

Abstract

Werner's syndrome, also known as "progeria adultorum", manifests itself in young adults. They appear older than their chronological age. Characteristically, there is atrophy in the distal extremities and the face. There is progressive scleropoikiloderma and hyperkeratosis on the foot soles. In the face, there is frequently a "bird-like" expression. Other characteristics are premature graying and early loss of hair, juvenile cataracts, hypogonadism, diabetic symptoms, arteriosclerosis, osteoporosis, small stature with characteristic features, muscle atrophy and cardiac abnormalities. The disease is inherited in an autosomal recessive way. Pathogenesis is unclear. In the following paper, we are reporting the case of a 29 year old saleswoman, who complained of cramps in the calves, and presented the typical symptoms of Werner's syndrome.

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Mesh:

Year:  1980        PMID: 7367844

Source DB:  PubMed          Journal:  Schweiz Med Wochenschr        ISSN: 0036-7672


  3 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.  Hereditary sclerosing poikiloderma.

Authors:  Hyo Jin Lee; Dong Hoon Shin; Jong Soo Choi; Ki Hong Kim
Journal:  J Korean Med Sci       Date:  2012-01-27       Impact factor: 2.153

3.  Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts.

Authors:  D Salk; E Bryant; K Au; H Hoehn; G M Martin
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

  3 in total

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