» Articles » PMID: 5820595

Cockayne's Syndrome. Report of Case with Necropsy Findings

Overview
Specialty Neurology
Date 1969 Sep 9
PMID 5820595
Citations 12
Authors
Affiliations
Soon will be listed here.
Citing Articles

Cognitive Decline and Other Late-Stage Neurologic Complications in Cockayne Syndrome.

Rajamani G, Stafki S, Daugherty A, Mantyh W, Littel H, Bruels C Neurol Clin Pract. 2024; 14(4):e200309.

PMID: 38808024 PMC: 11129329. DOI: 10.1212/CPJ.0000000000200309.


Movement Disorders and Spinal Cord Atrophy in Cockayne Syndrome with Prolonged Survival.

Planas-Ballve A, Morales-Briceno H, Crespo-Cuevas A, Fung V Mov Disord Clin Pract. 2021; 5(2):209-211.

PMID: 33999981 PMC: 6336154. DOI: 10.1002/mdc3.12588.


A possible cranio-oro-facial phenotype in Cockayne syndrome.

Bloch-Zupan A, Rousseaux M, Laugel V, Schmittbuhl M, Mathis R, Desforges E Orphanet J Rare Dis. 2013; 8:9.

PMID: 23311583 PMC: 3599377. DOI: 10.1186/1750-1172-8-9.


Neuroimaging in Cockayne syndrome.

Koob M, Laugel V, Durand M, Fothergill H, Dalloz C, Sauvanaud F AJNR Am J Neuroradiol. 2010; 31(9):1623-30.

PMID: 20522568 PMC: 7964976. DOI: 10.3174/ajnr.A2135.


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

Rapin I, Weidenheim K, Lindenbaum Y, Rosenbaum P, Merchant S, Krishna S J Child Neurol. 2006; 21(11):991-1006.

PMID: 17092472 PMC: 2772653. DOI: 10.1177/08830738060210110101.


References
1.
Cockayne E . Dwarfism with retinal atrophy and deafness. Arch Dis Child. 2010; 11(61):1-8. PMC: 1975412. DOI: 10.1136/adc.11.61.1. View

2.
Ohno T, Hirooka M . Renal lesions in Cockayne's syndrome. Tohoku J Exp Med. 1966; 89(2):151-66. DOI: 10.1620/tjem.89.151. View

3.
SPARK H . CACHECTIC DWARFISM RESEMBLING THE COCKAYNE-NEILL TYPE. J Pediatr. 1965; 66:41-7. DOI: 10.1016/s0022-3476(65)80336-5. View

4.
KEAY A, Oliver M, BOYD G . Progeria and atherosclerosis. Arch Dis Child. 1955; 30(153):410-4. PMC: 2011807. DOI: 10.1136/adc.30.153.410. View

5.
MacDONALD W, Fitch K, Lewis I . Cockayne's syndrome. An heredo-familial disorder of growth and development. Pediatrics. 1960; 25:997-1007. View