Literature DB >> 557874

Retinitis pigmentosa and a retinal vasculopathy of the Coats type.

W Banks Anderson, J A Wadsworth, M B Landers.   

Abstract

Retinitis pigmentosa is occasionally associated with a vasculopathy of the Coats type. Although the clinical appearance of the vaculopathy is similar to that seen in the usual patient iwth Coats's disease, cases associated with retinitis pigmentosa are usually bilateral, equally common in females, and are not seen in childhood. These findings suggest a different etiological process. We speculate that the etiology in such cases may be related to the vascular narrowing and slower circulation known to occur in some retinitis pigmentosa patients.

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Year:  1977        PMID: 557874     DOI: 10.1007/978-1-4899-5010-9_5

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  4 in total

1.  Retinitis pigmentosa: clinical observations and correlations.

Authors:  R C Pruett
Journal:  Trans Am Ophthalmol Soc       Date:  1983

Review 2.  Advanced Coats' disease.

Authors:  B G Haik
Journal:  Trans Am Ophthalmol Soc       Date:  1991

3.  X-linked dominant RPGR gene mutation in a familial Coats angiomatosis.

Authors:  Antonio Pizzuti; Enrica Marchionni; Marcella Nebbioso; Federica Franzone; Alessandro Lambiase; Maurizio La Cava; Fabiana Mallone
Journal:  BMC Ophthalmol       Date:  2021-01-14       Impact factor: 2.209

4.  Peripheral Inflammatory Yellow Exudative Retinal Coats-Like Vitreoretinopathy Misdiagnosed as Acute Retinal Necrosis in a Retinitis Pigmentosa Patient after Cataract Surgery.

Authors:  Lara Tran; Ioannis Papasavvas; Johannes Fleischhauer; Carl P Herbort
Journal:  Case Rep Ophthalmol       Date:  2021-06-18
  4 in total

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