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Multiple schwannomas, multiple nevi, and multiple vaginal leiomyomas: A new dominant syndrome

✍ Scribed by Gorlin, Robert J.; Koutlas, Ioannis G.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
59 KB
Volume
78
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19980616)78:1<76::aid-ajmg16>3.0.co;2-l

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✦ Synopsis


We report on a family of seven affected with a new syndrome of multiple deep schwannomas, multiple nevi (both intradermal and compound types), and multiple leiomyomas of the vagina. Inheritance is dominant, whether autosomal or X-linked cannot be determined at this time. The nevi, which are congenital, appear to be a marker for the syndrome. Both the schwannomas and leiomyomas do not manifest until adulthood.


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