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조로증

조로증(早老症,Progeria syndromes, Accelerated aging)은 빨리 늙는 병이다. 조로증의 원인으로는 DNA 복구에 문제가 생긴 경우 등이 있다. 여러 유형의 조로증이 있다.

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  • 모세혈관확장 운동실조(Ataxia telangiectasia)[1]
  • 블룸 증후군(Bloom syndrome)
  • 코케인 증후군(Cockayne's syndrome)
  • 판코니 빈혈증(Fanconi's anaemia)
  • 프로제리아(Progeria): 아동의 나이에 노인처럼 되는 질병[2][3]
  • 로트문드-톰슨 증후군(Rothmund-Thomson syndrome)[4][5]
  • 모발유황이영양증(황결핍성 모발 이영양증, Trichothiodystrophy)[6]
  • 베르너 증후군(Werner syndrome): 중년의 나이에 노인처럼 된다.
  • 색소피부건조증(Xeroderma pigmentosum)

같이 보기

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각주

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  1. Biton S, Dar I, Mittelman L, Pereg Y, Barzilai A, Shiloh Y (June 2006). “Nuclear ataxia-telangiectasia mutated (ATM) mediates the cellular response to DNA double strand breaks in human neuron-like cells”. 《J. Biol. Chem.》 281 (25): 17482–91. doi:10.1074/jbc.M601895200. PMID 16627474. 2009년 4월 25일에 원본 문서에서 보존된 문서. 2015년 11월 10일에 확인함. 
  2. Manju K, Muralikrishna B, Parnaik VK (July 2006). “Expression of disease-causing lamin A mutants impairs the formation of DNA repair foci”. 《J. Cell. Sci.》 119 (Pt 13): 2704–14. doi:10.1242/jcs.03009. PMID 16772334. 
  3. Scaffidi P, Misteli T (May 2006). “Lamin A-dependent nuclear defects in human aging”. 《Science》 312 (5776): 1059–63. doi:10.1126/science.1127168. PMC 1855250. PMID 16645051. 
  4. Brosh RM, Bohr VA (2007). “Human premature aging, DNA repair and RecQ helicases”. 《Nucleic Acids Res.》 35 (22): 7527–44. doi:10.1093/nar/gkm1008. PMC 2190726. PMID 18006573. 
  5. Kitao S, Shimamoto A, Goto M, 외. (May 1999). “Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome”. 《Nat. Genet.》 22 (1): 82–4. doi:10.1038/8788. PMID 10319867. 
  6. Kleijer WJ, Laugel V, Berneburg M, 외. (May 2008). “Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy”. 《DNA Repair (Amst.)》 7 (5): 744–50. doi:10.1016/j.dnarep.2008.01.014. PMID 18329345. 
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조로증
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