List of cutaneous conditions caused by mutations in keratins
This is a dynamic list and may never be able to satisfy particular standards for completeness. You can help by expanding it with reliably sourced entries.
See also: List of cutaneous conditions
There are many different keratin proteins normally expressed in the human integumentary system. Mutations in keratin proteins in the skin can cause disease.
Of note, other structural proteins in the epidermis of the skin that are closely related to keratins may also cause disease if mutated. Examples include:
Defective protein | Conditions(s) |
---|---|
Loricrin | Vohwinkel syndrome[nb 1] Progressive symmetric erythrokeratodermia |
Filaggrin | Ichthyosis vulgaris Atopic dermatitis |
Footnotes
- ↑ Vohwinkel syndrome may be caused by mutations in either loricrin or GJB2. This is an example of locus heterogeneity.
See also
- List of keratins expressed in the human integumentary system
- List of cutaneous conditions caused by problems with junctional proteins
- List of target antigens in pemphigoid
- List of target antigens in pemphigus
- Cutaneous conditions with immunofluorescence findings
- List of cutaneous conditions
- List of genes mutated in cutaneous conditions
- List of histologic stains that aid in diagnosis of cutaneous conditions
- Keratoderma
References
- Bolognia, Jean L.; et al. (2007). Dermatology. St. Louis: Mosby. ISBN 1-4160-2999-0.
- James, William D.; et al. (2006). Andrews' Diseases of the Skin: Clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.
This article is issued from Wikipedia - version of the 10/15/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.