Literature DB >> 2468771

Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies.

M A Patton1, F Giannelli, A J Francis, M Baraitser, B Harding, A J Williams.   

Abstract

Two patients with early onset Cockayne's syndrome are presented. In each case there was a striking failure of growth and developmental deterioration around six months of age. It has been suggested that early onset Cockayne's syndrome is a syndrome distinct from Cockayne's syndrome, but when the first patient died aged two years 10 months, examination of the brain showed a leucodystrohy with 'tigroid' demyelination similar to that reported in later onset cases of Cockayne's syndrome. Studies of the effects of UV irradiation on cultured fibroblasts from patients showed similar levels of inhibition of RNA synthesis to those seen in a control with Cockayne's syndrome. This evidence suggests it is appropriate to classify early onset Cockayne's syndrome with Cockayne's syndrome. Since there is a phenotypic overlap between early onset Cockayne's syndrome and COFS syndrome, they may both be classified within the same diagnostic group, but as yet no cellular studies with UV irradiation have been performed in COFS syndrome.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2468771      PMCID: PMC1015575          DOI: 10.1136/jmg.26.3.154

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  11 in total

1.  Abnormal kinetics of DNA synthesis in ultraviolet light-irradiated cells from patients with Cockayne's syndrome.

Authors:  A R Lehmann; S Kirk-Bell; L Mayne
Journal:  Cancer Res       Date:  1979-10       Impact factor: 12.701

2.  Prenatal diagnosis of Cockayne's syndrome.

Authors:  A R Lehmann; A J Francis; F Giannelli
Journal:  Lancet       Date:  1985-03-02       Impact factor: 79.321

3.  Cataracts, microcephaly, kyphosis, and limited joint movement in two siblings: a new syndrome.

Authors:  R B Lowry; R MacLean; D M McLean; B Tischler
Journal:  J Pediatr       Date:  1971-08       Impact factor: 4.406

4.  Three complementation groups in Cockayne syndrome.

Authors:  A R Lehmann
Journal:  Mutat Res       Date:  1982-12       Impact factor: 2.433

5.  Necropsy of original case of Lowry's syndrome.

Authors:  C L Dolman; V J Wright
Journal:  J Med Genet       Date:  1978-06       Impact factor: 6.318

6.  Autosomal recessive cerebro-oculo-facio-skeletal (COFS) syndrome.

Authors:  S D Pena; M H Shokeir
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

7.  The neuropathology of Cockayne's syndrome.

Authors:  J Moossy
Journal:  J Neuropathol Exp Neurol       Date:  1967-10       Impact factor: 3.685

8.  Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum.

Authors:  L V Mayne; A R Lehmann
Journal:  Cancer Res       Date:  1982-04       Impact factor: 12.701

9.  Effects of DNA damaging agents on cultured fibroblasts derived from patients with Cockayne syndrome.

Authors:  M H Wade; E H Chu
Journal:  Mutat Res       Date:  1979-01       Impact factor: 2.433

10.  Cockayne syndrome with early onset of manifestations.

Authors:  D B Moyer; P Marquis; M E Shertzer; B K Burton
Journal:  Am J Med Genet       Date:  1982-10
View more
  8 in total

1.  Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.

Authors:  J M Graham ; K Anyane-Yeboa; A Raams; E Appeldoorn; W J Kleijer; V H Garritsen; D Busch; T G Edersheim; N G Jaspers
Journal:  Am J Hum Genet       Date:  2001-07-03       Impact factor: 11.025

2.  Cranial CT and MRI in diseases with DNA repair defects.

Authors:  P Demaerel; B E Kendall; D Kingsley
Journal:  Neuroradiology       Date:  1992       Impact factor: 2.804

3.  Neuroimaging in Cockayne syndrome.

Authors:  M Koob; V Laugel; M Durand; H Fothergill; C Dalloz; F Sauvanaud; H Dollfus; I J Namer; J-L Dietemann
Journal:  AJNR Am J Neuroradiol       Date:  2010-06-03       Impact factor: 3.825

4.  Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.

Authors:  L B Meira; J M Graham; C R Greenberg; D B Busch; A T Doughty; D W Ziffer; D M Coleman; I Savre-Train; E C Friedberg
Journal:  Am J Hum Genet       Date:  2000-03-15       Impact factor: 11.025

5.  Cockayne syndrome: a diffusion tensor imaging and volumetric study.

Authors:  Mériam Koob; François Rousseau; Vincent Laugel; Nicolas Meyer; Jean-Paul Armspach; Nadine Girard; Jean-Louis Dietemann
Journal:  Br J Radiol       Date:  2016-09-19       Impact factor: 3.039

6.  Xeroderma pigmentosum--Cockayne syndrome complex: a further case.

Authors:  B C Hamel; A Raams; A R Schuitema-Dijkstra; P Simons; I van der Burgt; N G Jaspers; W J Kleijer
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

7.  Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity.

Authors:  C G Bönnemann; P Meinecke; H Reich
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

Review 8.  The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis).

Authors:  J L Tolmie; P Shillito; R Hughes-Benzie; J B Stephenson
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.