Journal Basic Info

  • Impact Factor: 1.809**
  • H-Index: 6
  • ISSN: 2474-1655
  • DOI: 10.25107/2474-1655
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Molecular Biology
  •  Sexual Health
  •  Orthopedic Surgery
  •  Orthopedics & Rheumatology
  •  Gastric Cancer
  •  Internal Medicine
  •  Pharmacology and Therapeutics
  •  Asthma

Abstract

Citation: Ann Clin Case Rep. 2022;7(1):2320.DOI: 10.25107/2474-1655.2320

Retinitis Pigmentosa and Ocular Motility Alterations: New Frontiers, Review

Arrico L*, Grimaldi C, Cecchetti D, Crevatin CA and Compagno S

Department of Sense Organs, Glaucoma Service, Clinical Ophthalmology, University of Rome “Sapienza”, Italy

*Correspondance to: Loredana Arrico 

 PDF  Full Text Review Article | Open Access

Abstract:

Purpose: To carry out a review of the literature on alterations in extraocular motility in Retinitis Pigmentosa (RP), focusing on the possible genetic basis of ocular alterations. Design: Systematic review Methods: The search of publications was carried out using the databases: Scopus, PubMed, Google Scholar, Web of Science, considering clinical cases, case reports, and systematic reviews of ocular motility alterations in the Retinitis Pigmentosa in the literature. The words: “ocular motility alterations, Retinitis Pigmentosa, orthoptic evaluation, case reports, clinical cases, systematic reviews” were used. Results: A total of 2 articles from 2006–2022 were retrieved: No other ocular motility alterations clinical cases linked to RP were found before. Particularly, a study conducted on patients affected by typical RP showed that there was an impaired motility in 50% of them. Since RP is a genetically determined disease, in reference to the studies analyzed, the absence of eye movement disorders in a percentage of the sample could be related to the different penetrance of the disease that determines the existence of healthy carriers. Conclusion: Therefore, it would be important to search for a possible correlation between the genetic mutations involved in this hereditary disorder and the deficits in extraocular motility, in order to make an early diagnosis of RP in genetically predisposed subjects. The existence of alterations of extraocular motility in subjects with RP, indicates that a careful orthoptic screening can allow a further contribution to an early diagnosis of this disease, especially in subjects with positive family history and healthy carriers.

Keywords:

Cite the Article:

Arrico L, Grimaldi C, Cecchetti D, Crevatin CA, Compagno S. Retinitis Pigmentosa and Ocular Motility Alterations: New Frontiers, Review. Ann Clin Case Rep. 2022; 7: 2320..

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