Difference between revisions of "Xeroderma pigmentosum"
Jump to navigation
Jump to search
(create) |
(No difference)
|
Revision as of 05:38, 5 September 2011
Xeroderma pigmentosum is an autosomal recessive disorder due to defective DNA repair.[1]
Associations
- Basal cell carcinoma.
- Others.
References
- ↑ Ramkumar, HL.; Brooks, BP.; Cao, X.; Tamura, D.; Digiovanna, JJ.; Kraemer, KH.; Chan, CC.. "Ophthalmic manifestations and histopathology of xeroderma pigmentosum: two clinicopathological cases and a review of the literature.". Surv Ophthalmol 56 (4): 348-61. doi:10.1016/j.survophthal.2011.03.001. PMID 21684361.