No.11886 a rare genetic condition characterized by an eruption of exposed skin occurring in childhood and photosensitivity with severe sunburn; inherited as a recessive autosomal trait in which DNA repair processes are defective so they are more likely to chromosome breaks and cancers when exposed to ultraviolet light
⭕️
❌
💾
| 🖊 | ☑️ |
| ⭕️ | [[ AnswerCalc[0] ]] % | A | [[ AnswerCalc[1] ]] |
|
|
|
|
|
|
|
|
💾
✔️
| [[ d.CommentTxt ]] |
| < | > |
| 🥇 |