Werner Syndrome, or adult progeria, is a rare autosomal recessive disorder caused by a mutation in the Werner Syndrome Gene belonging to the family of RecQ helicase.
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In current scenario, involving scientific research in diversified disciplines, it is necessary to publish several forms of case reports and scholarly papers. As a result, the importance of open access journals is growing significantly.Introduction.
Werner syndrome (WS) is a segmental progeria. It belongs to a small group of disorders characterized by accelerated aging. WS patients in their 20s and 30s display features similar but not identical to those of normal older individuals, including skin atrophy, graying and loss of hair, wrinkles, loss of fat, cataracts, atherosclerosis, and diabetes (reviewed in Yokote et al.
1). INTRODUCTION Werner syndrome (WS) is an autosomal recessive disorder characterized by premature onset and an accelerated rate of development of major geriatric diseases, including atherosclerosis, diabetes mellitus, osteoporosis, cataract and menopause, and further TRF analysis.
Introduction: Werner Syndrome, or adult progeria, is a rare autosomal recessive disorder caused by a mutation in the Werner Syndrome Gene belonging to the family of RecQ helicase. Malignant mesenchymal tumours and.
BackgroundThree pregnancies with male offspring in one family were complicated by severe polyhydramnios and prematurity. One fetus died; the other two had transient massive salt-wasting and. Introduction: Werner Syndrome, or adult progeria, is a rare autosomal recessive disorder caused by a mutation in the Werner Syndrome Gene belonging to the family of RecQ helicase.
Background Previous studies have suggested that the obstructive sleep apnea syndrome may be an important risk factor for stroke. It has not been determined, however, whether the syndrome is.