Difference between revisions of "Xeroderma pigmentosum"
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*[[Basal cell carcinoma]]. | *[[Basal cell carcinoma]]. | ||
*Others. | *Others. | ||
==See also== | |||
*[[Molecular pathology]]. | |||
==References== | ==References== | ||
Revision as of 12:41, 4 May 2012
Xeroderma pigmentosum is an autosomal recessive disorder due to defective DNA repair.[1]
Associations
- Basal cell carcinoma.
- Others.
See also
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.