Jump to content

Westerhof syndrome

Add links
From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Tom.Reding (talk | contribs) at 03:02, 19 May 2016 (→top: vauthors/veditors or enumerate multiple authors/editors (CS1 maintenance), WP:GenFixes using AWB). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Westerhof syndrome

Westerhof syndrome is a cutaneous condition inherited in an autosomal dominant fashion, characterized by congenital hypopigmented macules.[1]

See also

References

  1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 831. ISBN 1-4160-2999-0.


This Genodermatoses article is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Westerhof_syndrome&oldid=720984730"