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http://purl.uniprot.org/citations/28225726http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
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Purpose

Fabry disease is a rare lysosomal storage disorder with systemic involvement. The authors report on a large Fabry family with GLA p.M187R mutation and exhaustive ophthalmologic assessment.

Methods

Comprehensive systemic evaluation and genetic diagnosis were performed. Ophthalmologic evaluation included intraocular pressure/visual acuity measurement, refractometry, slit lamp examination, retinography, and optical coherence tomography. Three parameters quantified retinal vessel tortuosity: sum of angle metrics, product of angle distance, and triangular index. Calculations were semiautomatized using dedicated software.

Results

Ten individuals (2 males and 8 females) were described. Seventy-five percent had retinal vessel tortuosity. One hundred percent had cornea verticillata. Perimacular vessels were predominantly involved. The correlation between the right and left eye tortuosity measurements was very tight. A significant correlation between retinal vessel tortuosity and systemic severity measured by general Mainz Severity Score Index (MSSI), renal MSSI, and neurological MSSI but no cardiac MSSI was observed. Right sum of angle metrics value was an independent statistical predictor of the general-MSSI score in presence of age.

Conclusion

p.M187R mutation causes a severe systemic and ophthalmologic phenotype, in both male and female patients. Semiautomatic assessment of retinal vessel tortuosity is an objective and reproducible tool. All three parameters of tortuosity are closely associated with Fabry severity scores. Studies of larger series are being awaited to establish the role of retinal vessel tortuosity as a noninvasive marker of disease progression."xsd:string
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http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"Sodi A."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"Lopez D."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"Gimeno J.R."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"Rodriguez B."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"Rodriguez M.E."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"San Roman I."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"Caporossi O."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"Mecocci A."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/author"Zoppetti C."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/name"Retina"xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/pages"592-603"xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/title"COMPUTER ASSISTED RETINAL VESSEL TORTUOSITY EVALUATION IN NOVEL MUTATION FABRY DISEASE: Towards New Prognostic Markers."xsd:string
http://purl.uniprot.org/citations/28225726http://purl.uniprot.org/core/volume"37"xsd:string
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