Senter syndrome

Senter syndrome
Classification and external resources
OMIM 148210
DiseasesDB 32841

Senter syndrome (also known as "Desmons' syndrome")[1] 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 mental retardation.[2]

See also

References

  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 1-4160-2999-0.


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