Neonatal ichthyosis–sclerosing cholangitis syndrome
- Neonatal ichthyosis–sclerosing cholangitis syndrome
-
| Neonatal ichthyosis–sclerosing cholangitis syndrome |
| Classification and external resources |
| OMIM |
607626 |
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
- ^ 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.
Categories:
- Dermatology stubs
- Genodermatoses
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