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Results 1 - 6 of 6 for Cockayne syndrome type 2
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  1. ERCC8 gene 
    ... M, Hegele RA. CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new common polymorphism. J Hum Genet. 2004;49(1):61-63. doi: 10.1007/s10038-003-0107-2. Epub 2003 Dec 6. Citation on PubMed Kamiuchi ...
    https://medlineplus.gov/genetics/gene/ercc8 - Genetics
  2. Cockayne syndrome 
    ... a spectrum instead of distinct types. Cockayne syndrome type II is also known as ... Cockayne syndrome is estimated to occur in 2 to 3 per million newborns in the United ...
    https://medlineplus.gov/genetics/condition/cockayne-syndrome - Genetics
  3. Xeroderma pigmentosum 
    ... J Invest Dermatol. 2012 Mar;132(3 Pt 2):785-96. doi: 10.1038/jid.2011.426. Epub ... Cockayne syndrome and trichothiodystrophy. DNA Repair (Amst). 2008 May 3; ...
    https://medlineplus.gov/genetics/condition/xeroderma-pigmentosum - Genetics
  4. KRT14 gene 
    ... including the localized type (formerly called the Weber-Cockayne type) and a form known as the other generalized ... JA, Richard G, Sprecher E. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in ...
    https://medlineplus.gov/genetics/gene/krt14 - Genetics
  5. Trichothiodystrophy 
    ... repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy. DNA Repair (Amst). 2008 May 3; ...
    https://medlineplus.gov/genetics/condition/trichothiodystrophy - Genetics
  6. Metronidazole 
    ... your doctor if you or your child has Cockayne syndrome (an inherited condition that causes sensitivity to light, ...
    https://medlineplus.gov/druginfo/meds/a689011.html - Drugs and Supplements