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Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literature

✍ Scribed by Makoto Goto; Kiyoaki Tanimoto; Yoshihiko Horiuchi; Takehiko Sasazuki


Book ID
119839099
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
411 KB
Volume
19
Category
Article
ISSN
0009-9163

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The Marshall syndrome is an autosomal dominant trait comprising ocular abnormalities, sensorineural hearing loss, craniofacial anomalies, and anhidrotic ectodermal dysplasia. To our knowledge, only seven additional multigenerational families have been reported since the initial description of the di