Literature DB >> 8294592

Cockayne syndrome in two adult siblings.

H Miyauchi1, T Horio, T Akaeda, Y Asada, H R Chang, K Ishizaki, M Ikenaga.   

Abstract

Although survival beyond the second decade is unusual in patients who have Cockayne syndrome, we describe two brothers with the syndrome who are 42 and 55 years of age. Their cultured skin fibroblasts showed extreme UV sensitivity but had almost normal UV-induced unscheduled DNA synthesis. The patients were classified as genetic complementation group B after study of the recovery of RNA synthesis after UV irradiation of fused cells. Clinical phototesting revealed a reduced threshold for UVB erythema.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8294592     DOI: 10.1016/s0190-9622(94)70034-6

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  7 in total

Review 1.  Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity.

Authors:  James E Cleaver; Ernest T Lam; Ingrid Revet
Journal:  Nat Rev Genet       Date:  2009-10-07       Impact factor: 53.242

Review 2.  Cockayne syndrome in adults: review with clinical and pathologic study of a new case.

Authors:  Isabelle Rapin; Karen Weidenheim; Yelena Lindenbaum; Pearl Rosenbaum; Saumil N Merchant; Sindu Krishna; Dennis W Dickson
Journal:  J Child Neurol       Date:  2006-11       Impact factor: 1.987

3.  Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.

Authors:  T Itoh; J E Cleaver; M Yamaizumi
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

4.  UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.

Authors:  T Itoh; Y Fujiwara; T Ono; M Yamaizumi
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

Review 5.  Nucleotide excision repair and cancer.

Authors:  Diana Leibeling; Petra Laspe; Steffen Emmert
Journal:  J Mol Histol       Date:  2006-07-20       Impact factor: 3.156

6.  Genetic analysis of twenty-two patients with Cockayne syndrome.

Authors:  M Stefanini; H Fawcett; E Botta; T Nardo; A R Lehmann
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

7.  Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing.

Authors:  Nadège Calmels; Géraldine Greff; Cathy Obringer; Nadine Kempf; Claire Gasnier; Julien Tarabeux; Marguerite Miguet; Geneviève Baujat; Didier Bessis; Patricia Bretones; Anne Cavau; Béatrice Digeon; Martine Doco-Fenzy; Bérénice Doray; François Feillet; Jesus Gardeazabal; Blanca Gener; Sophie Julia; Isabel Llano-Rivas; Artur Mazur; Caroline Michot; Florence Renaldo-Robin; Massimiliano Rossi; Pascal Sabouraud; Boris Keren; Christel Depienne; Jean Muller; Jean-Louis Mandel; Vincent Laugel
Journal:  Orphanet J Rare Dis       Date:  2016-03-22       Impact factor: 4.123

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.