Verweise von und zu Xeroderma pigmentosum
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- Atrophodermia pigmentosa
- Eye diseases, skin changes
- Basal cell carcinomatosis
- Cockayne syndrome
- De sanctis-cacchione syndrome
- Dna repair
- Dna repair genes
- Dyschromatosis universalis hereditaria
- Ephelids
- ERCC2 Gene
- Fibroxanthoma atypical
- Spot darker
- Kaposi, moriz
- Lentigines syndromes
- Lioderma essentialis congenita
- Neurom fibrillar
- Plant tars
- Photocarcinogenesis
- Photosensitivity syndromes
- Pibi(d)s syndrome
- Porphyria erythropoetica congenita
- REV1 gene
- Back mutation
- Senilitas cutis praecox
- Teleangiectasia
- Teleangiectasia
- Trichothiodystrophy
- Familial cancer syndrome
- Tumor syndromes, hereditary
- Xerodermoid, pigmented
Verweise zu anderen Artikeln
- Acitretin
- Actinic keratosis
- Atrophy of the skin (overview)
- Basal cell carcinoma (overview)
- Darian sign
- Dermis
- De sanctis-cacchione syndrome
- Dna repair
- Dyschromia
- Ectropium
- Excision
- Familial atypical multiple birthmark and melanoma syndrome (FAMM)
- Goltz syndrome
- Scale
- Hydroa vacciniforme
- Isotretinoin
- Kaposi, moriz
- Cryosurgery
- Curettage
- Light protection
- Light stabilizers
- Lupus erythematosus systemic
- Maculopapular cutaneous mastocytosis
- Melanoma cutaneous
- Microstomy
- Peutz-jeghers syndrome
- Phenotype
- Squamous cell carcinoma of the skin
- Poikiloderma (overview)
- Polymorphic light eruption
- Porphyria erythropoetica congenita
- Progeria adultorum
- Retinoids
- REV1 gene
- Stratum basale
- Translesion DNA synthesis
- Xerodermoid, pigmented