Jump to content

Neonatal ichthyosis–sclerosing cholangitis syndrome

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Ozzie10aaaa (talk | contribs) at 21:03, 28 September 2019. The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Neonatal ichthyosis–sclerosing cholangitis syndrome
Other namesNISCH syndrome
SpecialtyDermatology

Neonatal ichthyosis–sclerosing cholangitis syndrome (also known as "NISCH syndrome"[1] and "ichthyosis–sclerosing cholangitis syndrome"[1]) is a cutaneous condition caused by mutations in the Claudin 1 gene.[1]

See also

References

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