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Senter syndrome

From Wikipedia, the free encyclopedia
Senter syndrome
Other namesDesmons' syndrome[1]
SpecialtyDermatology

Senter syndrome is a cutaneous condition characterized by similar skin changes and congenital hearing impairment to keratitis–ichthyosis–deafness syndrome, but is associated with glycogen storage leading to hepatomegaly, hepatic cirrhosis, growth failure and intellectual disability.[2]

See also

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References

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  1. ^ Virginia P. Sybert (9 June 2010). Genetic Skin Disorders. Oxford University Press US. pp. 126–. ISBN 978-0-19-539766-6. Retrieved 17 December 2010.
  2. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
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