Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (54)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by FITZSIMONS, R. B.
Right arrow Articles by BIRD, A. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by FITZSIMONS, R. B.
Right arrow Articles by BIRD, A. C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 110, No. 3, 631-648, 1987
© 1987 Guarantors of Brain


research-article

RETINAL VASCULAR ABNORMALITIES IN FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY

A GENERAL ASSOCIATION WITH GENETIC AND THERAPEUTIC IMPLICATIONS

ROBIN B. FITZSIMONS1,2,, E. B. GURWIN1 and A. C. BIRD1,

1Department of Clinical Ophthalmology, Institute of Ophthalmology Queen Square, London 2National Hospital for Nervous Diseases Queen Square, London

Correspondence to: Correspondence to: Dr R. Fitzsimons, 229 Macquarie Street, Sydney, NSW 2000, Australia (myology)

Correspondence to: Professor A. C. Bird, Institute of Ophthalmology, Moorfields Eye Hospital, City Road, London ECIV 2PD (ophthalmology).

Because of occasional reports of exudative retinal detachment with facioscapulohumeral muscular dystrophy (F SH) and deafness, we sought to determine by fluorescein angiography whether there is any general relationship between FSH muscular dystrophy and retinal vascular disease. Peripheral retinal capillary abnormalities, comprising telangiectasis, closure, leakage and microaneurysm formation, were demonstrated by angiography in 56 out of 75 individuals with clinical or genetic evidence of FSH. Only 3 patients had relevant ophthalmoscopic abnormalities of the posterior pole and in only 1 was there consequent visual loss. This study included (1) one FSH family in which the propositus was treated for exudative retinopathy and 13 other subjects had telangiectasis, and (2) 8 cases (including 3 parents of apparently ‘sporadic’ FSH cases) in which fluorescein angiography confirmed the abnormal genotype, even though clinical examination of skeletal muscle revealed no clear abnormality. There was no correlation between the severity of the muscle disease and the extent of the retinal vascular abnormality. Visual complications of telangiectasis, although rare, may present early in life and before there is overt evidence of muscle disease. Since visual loss may be preventable, ophthalmic examination should be undertaken on infants at risk of having the abnormal gene.

The findings support the hypothesis that retinal capillary abnormalities are an integral part of the FSH muscular dystrophy syndrome and raise the question as to whether analogous capillary abnormalities could be implicated in the pathogenesis of FSH muscle disease.

Received April 1, 1986. Revised June 19, 1986. Accepted June 26, 1986.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
DMMHome page
R. D. Wuebbles, M. L. Hanel, and P. L. Jones
FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy
Dis. Model. Mech., May 1, 2009; 2(5-6): 267 - 274.
[Abstract] [Full Text] [PDF]


Home page
ptjournalHome page
S. Pandya, W. M King, and R. Tawil
Facioscapulohumeral Dystrophy
Physical Therapy, January 1, 2008; 88(1): 105 - 113.
[Abstract] [Full Text] [PDF]


Home page
Arch OphthalmolHome page
C. L. Shields, J. Zahler, N. Falk, M. Furuta, R. C. Eagle Jr, L. E. B. Espinosa, P. R. Fischer, and J. A. Shields
Neovascular Glaucoma From Advanced Coats Disease as the Initial Manifestation of Facioscapulohumeral Dystrophy in a 2-Year-Old Child
Arch Ophthalmol, June 1, 2007; 125(6): 840 - 842.
[Full Text] [PDF]


Home page
NeurologyHome page
R. J. Osborne, S. Welle, S. L. Venance, C. A. Thornton, and R. Tawil
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
Neurology, February 20, 2007; 68(8): 569 - 577.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
O. F. Brouwer, G. W. Padberg, C. Wijmenga, and R. R. Frants
Facioscapulohumeral Muscular Dystrophy in Early Childhood
Arch Neurol, April 1, 1994; 51(4): 387 - 394.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.