Literature DB >> 7192807

Cockayne syndrome: an atypical case.

R M Kennedy, V D Rowe, J J Kepes.   

Abstract

We report a case of Cockayne syndrome with several atypical features. The patient displayed many of the typical features, including cachectic bird-headed dwarfism, photodermatitis, normal pressure hydrocephalus, and extraphyramidal and pyramidal tract signs. However, she also displayed the unusual and previously unreported features of late age at onset, relative stability until age 19, and fertility, with a successful pregnancy. Brain biopsy showed hypomyelination, no active demyelination, and fibrillary gliosis.

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Year:  1980        PMID: 7192807     DOI: 10.1212/wnl.30.12.1268

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  4 in total

Review 1.  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

2.  The neuropathy of Cockayne syndrome.

Authors:  A Vos; A Gabreëls-Festen; E Joosten; F Gabreëls; W Renier; R Mullaart
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

3.  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

4.  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

  4 in total

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