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Westerhof syndrome

From Wikipedia, the free encyclopedia
Westerhof syndrome
This condition is inherited in an autosomal dominant manner.
SpecialtyDermatology

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

See also

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References

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  1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 831. ISBN 978-1-4160-2999-1.
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