Westerhof syndrome
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| name = Westerhof syndrome
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| image =Autosomal dominant - en.svg
| caption =This condition is inherited in an autosomal dominant manner.
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| field = Dermatology
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Westerhof syndrome is a cutaneous condition inherited in an autosomal dominant fashion, characterized by congenital hypopigmented macules.{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages=831 |isbn=978-1-4160-2999-1 }}
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| OMIM = 154000
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Category:Genetic disorders with OMIM but no gene
Category:Syndromes affecting the skin
{{Genodermatoses-stub}}