OBJECTIVE AND IMPORTANCE:: Meningioma arising in Werner syndrome has been
described previously, but never in association with a mutation analysis. We present the first …

A 53-year-old man presented with a rare meningioma associated with Werner syndrome.
Screening brain magnetic resonance (MR) imaging with gadolinium had detected multiple …

Summary 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 …

Werner'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 …

We present two cases of Werner's syndrome associated with intracranial meningioma.
Characteristic clinical features of Werner's syndrome include short stature with slender …

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The correlation between mutations in the Werner's syndrome (WRN) gene and the
haplotypes of surrounding markers was studied in Japanese patients. We have elucidated …

Several patients with Werner's syndrome in a large family group in Sardinia were
ascertained three years ago and reported briefly by Rabbiosi and Borroni (1979). Since then …

Werner syndrome (WS) is an extremely rare, autosomal recessive segmental progeroid
disorder caused by biallelic pathogenic variants in the WRN, which encodes a …

Three primary lesions of malignant melanoma developed in a 44‐year‐old Japanese
woman with Werner syndrome. One lesion was on the right large pudental lip and the others …