Literature DB >> 655905

Normal pressure hydrocephalus. Recognition and relationship to neurological abnormalities in Cockayne's syndrome.

R A Brumback, F W Yoder, A D Andrews, G L Peck, J H Robbins.   

Abstract

Normal pressure hydrocephalus (NPH) in adults is a well-known cause of dementia. We describe NPH in children having the recessively inherited Cockayne's syndrome (CS). Cockayne's syndrome is characterized by cachectic dwarfism, neurological dysfunction, and cutaneous sunlight sensitivity. We noted that the NPH-associated triad of dementia, gait disturbance, and incontinence developed in CS patients. Computerized tomography of the brain in our four CS patients showed hydrocephalic enlargement of the brain ventricles greatest in the older patients. There was no evidence of cortical atrophy except in the one patient who had CS with xeroderma pigmentosum. Lumbar puncture and radionuclide cisternography in the two patients tested showed normal CSF pressure, with complete blockade to flow of radionuclide above the tentorium cerebelli, ventricular reflux, and delayed absorption. Studies of NPH in CS may elucidate the pathophysiology of NPH and methods to alter its sequelae.

Entities:  

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Year:  1978        PMID: 655905     DOI: 10.1001/archneur.1978.00500300011002

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  17 in total

Review 1.  Human DNA repair defects.

Authors:  C F Arlett
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

Review 2.  Ophthalmic manifestations and histopathology of xeroderma pigmentosum: two clinicopathological cases and a review of the literature.

Authors:  Hema L Ramkumar; Brian P Brooks; Xiaoguang Cao; Deborah Tamura; John J Digiovanna; Kenneth H Kraemer; Chi-Chao Chan
Journal:  Surv Ophthalmol       Date:  2011 Jul-Aug       Impact factor: 6.048

3.  Ultraviolet light-induced chromosomal aberrations in cultured cells from Cockayne syndrome and complementation group C xeroderma pigmentosum patients: lack of correlation with cancer susceptibility.

Authors:  L R Seguin; R E Tarone; K H Liao; J H Robbins
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

4.  Protein oxidative damage is associated with life expectancy of houseflies.

Authors:  R S Sohal; S Agarwal; A Dubey; W C Orr
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

5.  A clinical study of a family with Cockayne's syndrome.

Authors:  R Proops; A M Taylor; J Insley
Journal:  J Med Genet       Date:  1981-08       Impact factor: 6.318

Review 6.  Cockayne syndrome and xeroderma pigmentosum.

Authors:  I Rapin; Y Lindenbaum; D W Dickson; K H Kraemer; J H Robbins
Journal:  Neurology       Date:  2000-11-28       Impact factor: 9.910

7.  Hypersensitivity to DNA-damaging agents in cultured cells from patients with Usher's syndrome and Duchenne muscular dystrophy.

Authors:  J H Robbins; D A Scudiero; F Otsuka; R E Tarone; R A Brumback; J D Wirtschafter; R J Polinsky; S F Barrett; A N Moshell; R G Scarpinato
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-04       Impact factor: 10.154

8.  Ultraviolet-induced mutations in Cockayne syndrome cells are primarily caused by cyclobutane dimer photoproducts while repair of other photoproducts is normal.

Authors:  C N Parris; K H Kraemer
Journal:  Proc Natl Acad Sci U S A       Date:  1993-08-01       Impact factor: 11.205

9.  Distinctive skeletal dysplasia in Cockayne syndrome.

Authors:  M Cirillo Silengo; P Franceschini; R Bianco; M Biagioli; L Pastorin; N Vista; A Baldassar; L Benso
Journal:  Pediatr Radiol       Date:  1986

10.  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

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